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Erschienen in: Journal of Neurology 10/2023

09.07.2023 | Review

Diagnosis and management of Becker muscular dystrophy: the French guidelines

verfasst von: Armelle Magot, Karim Wahbi, France Leturcq, Sandrine Jaffre, Yann Péréon, Guilhem Sole, The French BMD working group

Erschienen in: Journal of Neurology | Ausgabe 10/2023

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Abstract

Becker muscular dystrophy (BMD) is one of the most frequent among neuromuscular diseases, affecting approximately 1 in 18,000 male births. It is linked to a genetic mutation on the X chromosome. In contrast to Duchenne muscular dystrophy, for which improved care and management have changed the prognosis and life expectancy of patients, few guidelines have been published for management of BMD. Many clinicians are inexperienced in managing the complications of this disease. In France, a committee of experts from a wide range of disciplines met in 2019 to establish recommendations, with the goal of improving care of patients with BMD. Here, we present the tools to provide diagnosis of BMD as quickly as possible and for differential diagnoses. Then, we describe the multidisciplinary approach essential for optimum management of BMD. We give recommendations for the initial assessment and follow-up of the neurological, respiratory, cardiac, and orthopedic consequences of males who present with BMD. Finally, we describe the optimal therapeutic management of these complications. We also provide guidance on cardiac management for female carriers.
Literatur
1.
Zurück zum Zitat Becker PE, Kiener F (1955) A new X-chromosomal muscular dystrophy. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr 193:427–448PubMedCrossRef Becker PE, Kiener F (1955) A new X-chromosomal muscular dystrophy. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr 193:427–448PubMedCrossRef
2.
Zurück zum Zitat Bushby KM, Thambyayah M, Gardner-Medwin D (1991) Prevalence and incidence of Becker muscular dystrophy. Lancet 337:1022–1024PubMedCrossRef Bushby KM, Thambyayah M, Gardner-Medwin D (1991) Prevalence and incidence of Becker muscular dystrophy. Lancet 337:1022–1024PubMedCrossRef
3.
Zurück zum Zitat Koenig M, Hoffman EP, Bertelson CJ et al (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509–517PubMedCrossRef Koenig M, Hoffman EP, Bertelson CJ et al (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509–517PubMedCrossRef
4.
Zurück zum Zitat Hoffman EP, Brown RH, Kunkel LM (1987) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51:919–928PubMedCrossRef Hoffman EP, Brown RH, Kunkel LM (1987) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51:919–928PubMedCrossRef
5.
Zurück zum Zitat Yazaki M, Yoshida K, Nakamura A et al (1999) Clinical characteristics of aged Becker muscular dystrophy patients with onset after 30 years. Eur Neurol 42:145–149PubMedCrossRef Yazaki M, Yoshida K, Nakamura A et al (1999) Clinical characteristics of aged Becker muscular dystrophy patients with onset after 30 years. Eur Neurol 42:145–149PubMedCrossRef
6.
Zurück zum Zitat Doriguzzi C, Palmucci L, Mongini T et al (1993) Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. J Neurol 240:269–271PubMedCrossRef Doriguzzi C, Palmucci L, Mongini T et al (1993) Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. J Neurol 240:269–271PubMedCrossRef
7.
Zurück zum Zitat Viggiano E, Picillo E, Ergoli M, Cirillo A, Del Gaudio S, Politano L (2017) Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. J Gene Med 19(4):e2952CrossRef Viggiano E, Picillo E, Ergoli M, Cirillo A, Del Gaudio S, Politano L (2017) Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. J Gene Med 19(4):e2952CrossRef
8.
Zurück zum Zitat Yoshioka M, Yorifuji T, Mituyoshi I (1998) Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy. Clin Genet 53:102–107PubMedCrossRef Yoshioka M, Yorifuji T, Mituyoshi I (1998) Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy. Clin Genet 53:102–107PubMedCrossRef
9.
Zurück zum Zitat Hoogerwaard EM, Bakker E, Ippel PF et al (1999) Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study. Lancet 353:2116–2119PubMedCrossRef Hoogerwaard EM, Bakker E, Ippel PF et al (1999) Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study. Lancet 353:2116–2119PubMedCrossRef
10.
Zurück zum Zitat Mercier S, Toutain A, Toussaint A et al (2013) Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age. Eur J Hum Genet 21:855–863PubMedPubMedCentralCrossRef Mercier S, Toutain A, Toussaint A et al (2013) Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age. Eur J Hum Genet 21:855–863PubMedPubMedCentralCrossRef
11.
Zurück zum Zitat Birnkrant DJ, Bushby K, Bann CM, Apkon SD, Blackwell A, Brumbaugh D, Case LE, Clemens PR, Hadjiyannakis S, Pandya S, Street N, Tomezsko J, Wagner KR, Ward LM, Weber DR, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol 17(3):251–267PubMedPubMedCentralCrossRef Birnkrant DJ, Bushby K, Bann CM, Apkon SD, Blackwell A, Brumbaugh D, Case LE, Clemens PR, Hadjiyannakis S, Pandya S, Street N, Tomezsko J, Wagner KR, Ward LM, Weber DR, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol 17(3):251–267PubMedPubMedCentralCrossRef
12.
Zurück zum Zitat Birnkrant DJ, Bushby K, Bann CM, Alman BA, Apkon SD, Blackwell A, Case LE, Cripe L, Hadjiyannakis S, Olson AK, Sheehan DW, Bolen J, Weber DR, Ward LM, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. Lancet Neurol 17(4):347–361PubMedPubMedCentralCrossRef Birnkrant DJ, Bushby K, Bann CM, Alman BA, Apkon SD, Blackwell A, Case LE, Cripe L, Hadjiyannakis S, Olson AK, Sheehan DW, Bolen J, Weber DR, Ward LM, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. Lancet Neurol 17(4):347–361PubMedPubMedCentralCrossRef
13.
Zurück zum Zitat Birnkrant DJ, Bushby K, Bann CM, Apkon SD, Blackwell A, Colvin MK, Cripe L, Herron AR, Kennedy A, Kinnett K, Naprawa J, Noritz G, Poysky J, Street N, Trout CJ, Weber DR, Ward LM, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan. Lancet Neurol 17(5):445–455PubMedPubMedCentralCrossRef Birnkrant DJ, Bushby K, Bann CM, Apkon SD, Blackwell A, Colvin MK, Cripe L, Herron AR, Kennedy A, Kinnett K, Naprawa J, Noritz G, Poysky J, Street N, Trout CJ, Weber DR, Ward LM, DMD Care Considerations Working Group (2018) Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan. Lancet Neurol 17(5):445–455PubMedPubMedCentralCrossRef
15.
Zurück zum Zitat Taglia A, Petillo R, D’Ambrosio P, Picillo E, Torella A, Orsini C, Ergoli M, Scutifero M, Passamano L, Palladino A, Nigro G, Politano L (2015) Clinical features of patients with dystrophinopathy sharing the 45–55 exon deletion of DMD gene. Acta Myol 34(1):9–13PubMedPubMedCentral Taglia A, Petillo R, D’Ambrosio P, Picillo E, Torella A, Orsini C, Ergoli M, Scutifero M, Passamano L, Palladino A, Nigro G, Politano L (2015) Clinical features of patients with dystrophinopathy sharing the 45–55 exon deletion of DMD gene. Acta Myol 34(1):9–13PubMedPubMedCentral
16.
Zurück zum Zitat Hermans MCE, Pinto YM, Merkies ISJ et al (2010) Hereditary muscular dystrophies and the heart. Neuromuscul Disord 20:479–492PubMedCrossRef Hermans MCE, Pinto YM, Merkies ISJ et al (2010) Hereditary muscular dystrophies and the heart. Neuromuscul Disord 20:479–492PubMedCrossRef
17.
Zurück zum Zitat Melacini P, Fanin M, Danieli GA et al (1996) Myocardial involvement is very frequent among patients affected with subclinical Becker’s muscular dystrophy. Circulation 94:3168–3175PubMedCrossRef Melacini P, Fanin M, Danieli GA et al (1996) Myocardial involvement is very frequent among patients affected with subclinical Becker’s muscular dystrophy. Circulation 94:3168–3175PubMedCrossRef
18.
Zurück zum Zitat Mavrogeni S, Markousis-Mavrogenis G, Papavasiliou A et al (2015) Cardiac involvement in Duchenne and Becker muscular dystrophy. World J Cardiol 7:410–414PubMedPubMedCentralCrossRef Mavrogeni S, Markousis-Mavrogenis G, Papavasiliou A et al (2015) Cardiac involvement in Duchenne and Becker muscular dystrophy. World J Cardiol 7:410–414PubMedPubMedCentralCrossRef
19.
Zurück zum Zitat Ferlini A, Sewry C, Melis MA et al (1999) X-linked dilated cardiomyopathy and the dystrophin gene. Neuromuscul Disord 9:339–346PubMedCrossRef Ferlini A, Sewry C, Melis MA et al (1999) X-linked dilated cardiomyopathy and the dystrophin gene. Neuromuscul Disord 9:339–346PubMedCrossRef
20.
Zurück zum Zitat Mori-Yoshimura M, Mizuno Y, Yoshida S, Ishihara N, Minami N, Morimoto E, Maruo K, Nonaka I, Komaki H, Nishino I, Sekiguchi M, Sato N, Takeda S, Takahashi Y (2019) Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy. Neuromuscul Disord 29(12):930–939PubMedCrossRef Mori-Yoshimura M, Mizuno Y, Yoshida S, Ishihara N, Minami N, Morimoto E, Maruo K, Nonaka I, Komaki H, Nishino I, Sekiguchi M, Sato N, Takeda S, Takahashi Y (2019) Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy. Neuromuscul Disord 29(12):930–939PubMedCrossRef
21.
Zurück zum Zitat Young HK, Barton BA, Waisbren S, Portales Dale L, Ryan MM, Webster RI, North KN (2008) Cognitive and psychological profile of males with Becker muscular dystrophy. J Child Neurol 23(2):155–162PubMedCrossRef Young HK, Barton BA, Waisbren S, Portales Dale L, Ryan MM, Webster RI, North KN (2008) Cognitive and psychological profile of males with Becker muscular dystrophy. J Child Neurol 23(2):155–162PubMedCrossRef
22.
Zurück zum Zitat Hinton VJ, Nereo NE, Fee RJ, Cyrulnik SE (2006) Social behavior problems in boys with Duchenne muscular dystrophy. J Dev Behav Pediatr 27(6):470–476PubMedPubMedCentralCrossRef Hinton VJ, Nereo NE, Fee RJ, Cyrulnik SE (2006) Social behavior problems in boys with Duchenne muscular dystrophy. J Dev Behav Pediatr 27(6):470–476PubMedPubMedCentralCrossRef
23.
Zurück zum Zitat Cyrulnik SE, Fee RJ, Batchelder A, Kiefel J, Goldstein E, Hinton VJ (2008) Cognitive and adaptive deficits in young children with Duchenne muscular dystrophy (DMD). J Int Neuropsychol Soc 14(5):853–861PubMedCrossRef Cyrulnik SE, Fee RJ, Batchelder A, Kiefel J, Goldstein E, Hinton VJ (2008) Cognitive and adaptive deficits in young children with Duchenne muscular dystrophy (DMD). J Int Neuropsychol Soc 14(5):853–861PubMedCrossRef
24.
Zurück zum Zitat Steele M, Taylor E, Young C, McGrath P, Lyttle BD, Davidson B (2008) Mental health of children and adolescents with Duchenne muscular dystrophy. Dev Med Child Neurol 50(8):638–639PubMedCrossRef Steele M, Taylor E, Young C, McGrath P, Lyttle BD, Davidson B (2008) Mental health of children and adolescents with Duchenne muscular dystrophy. Dev Med Child Neurol 50(8):638–639PubMedCrossRef
25.
Zurück zum Zitat Pascual-Morena C, Cavero-Redondo I, Álvarez-Bueno C, Jiménez-López E, Saz-Lara A, Martínez-García I, Martínez-Vizcaíno V (2023) Global prevalence of intellectual developmental disorder in dystrophinopathies: a systematic review and meta-analysis. Dev Med Child Neurol 65(6):734–744PubMedCrossRef Pascual-Morena C, Cavero-Redondo I, Álvarez-Bueno C, Jiménez-López E, Saz-Lara A, Martínez-García I, Martínez-Vizcaíno V (2023) Global prevalence of intellectual developmental disorder in dystrophinopathies: a systematic review and meta-analysis. Dev Med Child Neurol 65(6):734–744PubMedCrossRef
26.
Zurück zum Zitat Pascual-Morena C, Cavero-Redondo I, Reina-Gutiérrez S, Saz-Lara A, López-Gil JF, Martínez-Vizcaíno V (2022) Prevalence of neuropsychiatric disorders in Duchenne and Becker muscular dystrophies: a systematic review and meta-analysis. Arch Phys Med Rehabil 103(12):2444–2453PubMedCrossRef Pascual-Morena C, Cavero-Redondo I, Reina-Gutiérrez S, Saz-Lara A, López-Gil JF, Martínez-Vizcaíno V (2022) Prevalence of neuropsychiatric disorders in Duchenne and Becker muscular dystrophies: a systematic review and meta-analysis. Arch Phys Med Rehabil 103(12):2444–2453PubMedCrossRef
27.
Zurück zum Zitat Pascual-Morena C, Martínez-Vizcaíno V, Saz-Lara A, López-Gil JF, Fernández-Bravo-Rodrigo J, Cavero-Redondo I (2022) Epileptic disorders in Becker and Duchenne muscular dystrophies: a systematic review and meta-analysis. J Neurol 269(7):3461–3469PubMedCrossRef Pascual-Morena C, Martínez-Vizcaíno V, Saz-Lara A, López-Gil JF, Fernández-Bravo-Rodrigo J, Cavero-Redondo I (2022) Epileptic disorders in Becker and Duchenne muscular dystrophies: a systematic review and meta-analysis. J Neurol 269(7):3461–3469PubMedCrossRef
28.
Zurück zum Zitat Daoud F, Angeard N, Demerre B et al (2009) Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression. Hum Mol Genet 18:3779–3794PubMedCrossRef Daoud F, Angeard N, Demerre B et al (2009) Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression. Hum Mol Genet 18:3779–3794PubMedCrossRef
29.
Zurück zum Zitat Wang L, Chen M, He R, Sun Y, Yang J, Xiao L, Cao J, Zhang H, Zhang C (2017) Serum creatinine distinguishes Duchenne muscular dystrophy from Becker muscular dystrophy in patients aged ≤ 3 years: a retrospective study. Front Neurol 8(8):196PubMedPubMedCentralCrossRef Wang L, Chen M, He R, Sun Y, Yang J, Xiao L, Cao J, Zhang H, Zhang C (2017) Serum creatinine distinguishes Duchenne muscular dystrophy from Becker muscular dystrophy in patients aged ≤ 3 years: a retrospective study. Front Neurol 8(8):196PubMedPubMedCentralCrossRef
31.
Zurück zum Zitat Beltran Papsdorf T, Howard JF, Chahin N (2015) Late-onset Becker muscular dystrophy: refining the clinical features and electrophysiological findings. Muscle Nerve 15:1–3 Beltran Papsdorf T, Howard JF, Chahin N (2015) Late-onset Becker muscular dystrophy: refining the clinical features and electrophysiological findings. Muscle Nerve 15:1–3
32.
Zurück zum Zitat Tasca G, Iannaccone E, Monforte M et al (2012) Muscle MRI in Becker muscular dystrophy. Neuromuscul Disord 22:100–106CrossRef Tasca G, Iannaccone E, Monforte M et al (2012) Muscle MRI in Becker muscular dystrophy. Neuromuscul Disord 22:100–106CrossRef
33.
Zurück zum Zitat Uro-Soste E, Fernandez C, Authier FJ, Bassez G, Butori C, Chapon F, Delisle MB, Dubourg O, Feasson L, Gherardi R, Lacroix C, Laquerriere A, Letournel F, Magy L, Maisonobe T, Marcorelles P, Maurage CA, Mezin P, Mussini JM, Penisson-Besnier I, Romero NB, Streichenberger N, Vallat JM, Viennet G, Vital A, Voit T, Boucharef W, Figarella-Branger D (2010) Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l’Association française contre les myopathies. Rev Neurol (Paris) 166(5):477–485PubMedCrossRef Uro-Soste E, Fernandez C, Authier FJ, Bassez G, Butori C, Chapon F, Delisle MB, Dubourg O, Feasson L, Gherardi R, Lacroix C, Laquerriere A, Letournel F, Magy L, Maisonobe T, Marcorelles P, Maurage CA, Mezin P, Mussini JM, Penisson-Besnier I, Romero NB, Streichenberger N, Vallat JM, Viennet G, Vital A, Voit T, Boucharef W, Figarella-Branger D (2010) Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l’Association française contre les myopathies. Rev Neurol (Paris) 166(5):477–485PubMedCrossRef
34.
Zurück zum Zitat Muscle Biopsy: a practical approach. V Dubrowitz, C Sewry, A Oldfors. Fourth edition, Saunders Ed 2013. Muscle Biopsy: a practical approach. V Dubrowitz, C Sewry, A Oldfors. Fourth edition, Saunders Ed 2013.
35.
Zurück zum Zitat Na SJ, Kim WJ, Kim SM et al (2013) Clinical, immunohistochemical, Western blot, and genetic analysis in dystrophinopathy. J Clin Neurosci 20:1099–1105PubMedCrossRef Na SJ, Kim WJ, Kim SM et al (2013) Clinical, immunohistochemical, Western blot, and genetic analysis in dystrophinopathy. J Clin Neurosci 20:1099–1105PubMedCrossRef
36.
Zurück zum Zitat Ripolone M, Velardo D, Mondello S, Zanotti S, Magri F, Minuti E, Cazzaniga S, Fortunato F, Ciscato P, Tiberio F, Sciacco M, Moggio M, Bettica P, Comi GP (2022) Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy. Acta Neuropathol Commun 10(1):48PubMedPubMedCentralCrossRef Ripolone M, Velardo D, Mondello S, Zanotti S, Magri F, Minuti E, Cazzaniga S, Fortunato F, Ciscato P, Tiberio F, Sciacco M, Moggio M, Bettica P, Comi GP (2022) Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy. Acta Neuropathol Commun 10(1):48PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat Anthony K, Arechavala-Gomeza V, Taylor LE et al (2014) Dystrophin quantification: biological and translational research implications. Neurology 83:2062–2069PubMedPubMedCentralCrossRef Anthony K, Arechavala-Gomeza V, Taylor LE et al (2014) Dystrophin quantification: biological and translational research implications. Neurology 83:2062–2069PubMedPubMedCentralCrossRef
38.
Zurück zum Zitat Chevron MP, Tuffery S, Echenne B, Demaille J, Claustres M (1992) Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining. Neuromuscul Disord 2(1):47–50PubMedCrossRef Chevron MP, Tuffery S, Echenne B, Demaille J, Claustres M (1992) Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining. Neuromuscul Disord 2(1):47–50PubMedCrossRef
39.
Zurück zum Zitat Haginoya K, Yamamoto K, Iinuma K, Yanagisawa T, Ichinohasama Y, Shimmoto M, Suzuki Y, Tada K (1991) Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy. J Neurol 238(7):375–378PubMedCrossRef Haginoya K, Yamamoto K, Iinuma K, Yanagisawa T, Ichinohasama Y, Shimmoto M, Suzuki Y, Tada K (1991) Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy. J Neurol 238(7):375–378PubMedCrossRef
40.
Zurück zum Zitat Pegoraro E, Schimke RN, Garcia C et al (1995) Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei. Neurology 45:677–690PubMedCrossRef Pegoraro E, Schimke RN, Garcia C et al (1995) Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei. Neurology 45:677–690PubMedCrossRef
41.
Zurück zum Zitat Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM (1988) An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2(1):90–95PubMedCrossRef Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM (1988) An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2(1):90–95PubMedCrossRef
42.
Zurück zum Zitat Bello L, Campadello P, Barp A, Fanin M, Semplicini C, Sorarù G, Caumo L, Calore C, Angelini C, Pegoraro E (2016) Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies. Sci Rep 1(6):32439CrossRef Bello L, Campadello P, Barp A, Fanin M, Semplicini C, Sorarù G, Caumo L, Calore C, Angelini C, Pegoraro E (2016) Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies. Sci Rep 1(6):32439CrossRef
43.
Zurück zum Zitat Leturcq F, Tuffery-Giraud S (2015) Aspects génétiques et moléculaires des dystrophinopathies. Arch Pediatr 22(12 Suppl 1):12S3-12S11PubMedCrossRef Leturcq F, Tuffery-Giraud S (2015) Aspects génétiques et moléculaires des dystrophinopathies. Arch Pediatr 22(12 Suppl 1):12S3-12S11PubMedCrossRef
44.
Zurück zum Zitat Aartsma-Rus A, Ginjaar IB, Bushby K (2016) The importance of genetic diagnosis for Duchenne muscular dystrophy. J Med Genet 53(3):145–151PubMedCrossRef Aartsma-Rus A, Ginjaar IB, Bushby K (2016) The importance of genetic diagnosis for Duchenne muscular dystrophy. J Med Genet 53(3):145–151PubMedCrossRef
45.
Zurück zum Zitat Muntoni F, Torelli S, Ferlini A (2003) Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet 44:731–740CrossRef Muntoni F, Torelli S, Ferlini A (2003) Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet 44:731–740CrossRef
46.
Zurück zum Zitat Tuffery-Giraud S, Béroud C, Leturcq F et al (2009) Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase. Hum Mutat 30:934–945PubMedCrossRef Tuffery-Giraud S, Béroud C, Leturcq F et al (2009) Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase. Hum Mutat 30:934–945PubMedCrossRef
47.
Zurück zum Zitat Janssen B, Hartmann C, Scholz V et al (2005) MLPA analysis for the detection of deletions, duplications and complex réarrangements in the dystrophin gene: potential and pitfalls. Neurogenetics 6:29–35PubMedCrossRef Janssen B, Hartmann C, Scholz V et al (2005) MLPA analysis for the detection of deletions, duplications and complex réarrangements in the dystrophin gene: potential and pitfalls. Neurogenetics 6:29–35PubMedCrossRef
48.
Zurück zum Zitat Biancalana V, Laporte J (2015) Diagnostic use of massively parallel sequencing in neuromuscular diseases: towards an integrated diagnosis. J Neuromuscul Dis 2:87–92 Biancalana V, Laporte J (2015) Diagnostic use of massively parallel sequencing in neuromuscular diseases: towards an integrated diagnosis. J Neuromuscul Dis 2:87–92
49.
Zurück zum Zitat Tuffery-Giraud S, Saquet C, Thorel D et al (2005) Mutation Spectrum leading to an attenuated phenotype in dystrophinopathies. Eur J Hum Genet 13:1254–1260PubMedCrossRef Tuffery-Giraud S, Saquet C, Thorel D et al (2005) Mutation Spectrum leading to an attenuated phenotype in dystrophinopathies. Eur J Hum Genet 13:1254–1260PubMedCrossRef
50.
Zurück zum Zitat Schwartz M, Hertz JM, Sveen ML et al (2005) LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Neurology 64:1635–1637PubMedCrossRef Schwartz M, Hertz JM, Sveen ML et al (2005) LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Neurology 64:1635–1637PubMedCrossRef
51.
Zurück zum Zitat Bushby KM, Collins J, Hicks D (2014) Collagen type VI myopathies. Adv Exp Med Biol 802:185–199PubMedCrossRef Bushby KM, Collins J, Hicks D (2014) Collagen type VI myopathies. Adv Exp Med Biol 802:185–199PubMedCrossRef
52.
Zurück zum Zitat Domingos J, Sarkozy A, Scoto M, Muntoni F (2017) Dystrophinopathies and Limb-Girdle muscular dystrophies. Neuropediatrics 48(4):262–272PubMedCrossRef Domingos J, Sarkozy A, Scoto M, Muntoni F (2017) Dystrophinopathies and Limb-Girdle muscular dystrophies. Neuropediatrics 48(4):262–272PubMedCrossRef
53.
Zurück zum Zitat DeSimone AM, Pakula A, Lek A, Emerson CP Jr (2017) Facioscapulohumeral muscular dystrophy. Compr Physiol 7(4):1229–1279PubMedCrossRef DeSimone AM, Pakula A, Lek A, Emerson CP Jr (2017) Facioscapulohumeral muscular dystrophy. Compr Physiol 7(4):1229–1279PubMedCrossRef
54.
Zurück zum Zitat Selva-O’Callaghan A, Pinal-Fernandez I, Trallero-Araguás E, Milisenda JC, Grau-Junyent JM, Mammen AL (2018) Classification and management of adult inflammatory myopathies. Lancet Neurol 17(9):816–828PubMedCrossRef Selva-O’Callaghan A, Pinal-Fernandez I, Trallero-Araguás E, Milisenda JC, Grau-Junyent JM, Mammen AL (2018) Classification and management of adult inflammatory myopathies. Lancet Neurol 17(9):816–828PubMedCrossRef
55.
Zurück zum Zitat Juntas Morales R, Pageot N, Taieb G, Camu W (2017) Adult-onset spinal muscular atrophy: an update. Rev Neurol (Paris) 173(5):308–319PubMedCrossRef Juntas Morales R, Pageot N, Taieb G, Camu W (2017) Adult-onset spinal muscular atrophy: an update. Rev Neurol (Paris) 173(5):308–319PubMedCrossRef
57.
Zurück zum Zitat Angelini C, Marozzo R, Pegoraro V (2019) Current and emerging therapies in Becker muscular dystrophy (BMD). Acta Myol 38(3):172–179PubMedPubMedCentral Angelini C, Marozzo R, Pegoraro V (2019) Current and emerging therapies in Becker muscular dystrophy (BMD). Acta Myol 38(3):172–179PubMedPubMedCentral
58.
Zurück zum Zitat Maggi L, Moscatelli M, Frangiamore R, Mazzi F, Verri M, De Luca A, Pasanisi MB, Baranello G, Tramacere I, Chiapparini L, Bruzzone MG, Mantegazza R, Aquino D (2020) Quantitative muscle MRI protocol as possible biomarker in becker muscular dystrophy. Clin Neuroradiol 31:257–266PubMedCrossRef Maggi L, Moscatelli M, Frangiamore R, Mazzi F, Verri M, De Luca A, Pasanisi MB, Baranello G, Tramacere I, Chiapparini L, Bruzzone MG, Mantegazza R, Aquino D (2020) Quantitative muscle MRI protocol as possible biomarker in becker muscular dystrophy. Clin Neuroradiol 31:257–266PubMedCrossRef
59.
Zurück zum Zitat McDonald CM, Henricson EK, Abresch RT et al (2013) The 6-minute walk test and other clinical endpoints in Duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve 48:357–368PubMedPubMedCentralCrossRef McDonald CM, Henricson EK, Abresch RT et al (2013) The 6-minute walk test and other clinical endpoints in Duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve 48:357–368PubMedPubMedCentralCrossRef
60.
Zurück zum Zitat Florence JM, Pandya S, King WM et al (1984) Clinical trials in Duchenne dystrophy. Standardization and reliability of evaluation procedures. Phys Ther 64(1):41–45PubMedCrossRef Florence JM, Pandya S, King WM et al (1984) Clinical trials in Duchenne dystrophy. Standardization and reliability of evaluation procedures. Phys Ther 64(1):41–45PubMedCrossRef
61.
Zurück zum Zitat Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley R, Miller JP, Province MA (1983) Clinical investigation in Duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history. Muscle Nerve 6(2):91–103PubMedCrossRef Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley R, Miller JP, Province MA (1983) Clinical investigation in Duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history. Muscle Nerve 6(2):91–103PubMedCrossRef
62.
Zurück zum Zitat Vignos PJ Jr, Spencer GE Jr, Archibald KC (1963) Management of progressive muscular dystrophy in childhood. JAMA 184:89–96PubMedCrossRef Vignos PJ Jr, Spencer GE Jr, Archibald KC (1963) Management of progressive muscular dystrophy in childhood. JAMA 184:89–96PubMedCrossRef
63.
Zurück zum Zitat Vuillerot C, Rippert P, Roche S, Bérard C, Margirier F, de Lattre C, Poirot I, Berruyer A, Tiffreau V, Fournier-Mehouas M, Bouhour F, Urtizberea JA, Renders A, Ecochard R, Le groupe d’étude NM-Score (2013) Development and validation of a motor function classification in patients with neuromuscular disease: the NM-score. Ann Phys Rehabil Med 56(9–10):673–686PubMedCrossRef Vuillerot C, Rippert P, Roche S, Bérard C, Margirier F, de Lattre C, Poirot I, Berruyer A, Tiffreau V, Fournier-Mehouas M, Bouhour F, Urtizberea JA, Renders A, Ecochard R, Le groupe d’étude NM-Score (2013) Development and validation of a motor function classification in patients with neuromuscular disease: the NM-score. Ann Phys Rehabil Med 56(9–10):673–686PubMedCrossRef
64.
Zurück zum Zitat Vuillerot C, Meilleur KG, Jain M, Waite M, Wu T, Linton M, Datsgir J, Donkervoort S, Leach ME, Rutkowski A, Rippert P, Payan C, Iwaz J, Hamroun D, Bérard C, Poirot I, Bönnemann CG (2014) English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseases. Arch Phys Med Rehabil 95(11):2064-2070.e1PubMedPubMedCentralCrossRef Vuillerot C, Meilleur KG, Jain M, Waite M, Wu T, Linton M, Datsgir J, Donkervoort S, Leach ME, Rutkowski A, Rippert P, Payan C, Iwaz J, Hamroun D, Bérard C, Poirot I, Bönnemann CG (2014) English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseases. Arch Phys Med Rehabil 95(11):2064-2070.e1PubMedPubMedCentralCrossRef
65.
Zurück zum Zitat De Lattre C, Payan C, Vuillerot C, Rippert P, de Castro D, Bérard C, Poirot I (2013) Motor function measure: validation of a short form for young children with neuromuscular diseases. Arch Phys Med Rehabil 94(11):2218–2226PubMedCrossRef De Lattre C, Payan C, Vuillerot C, Rippert P, de Castro D, Bérard C, Poirot I (2013) Motor function measure: validation of a short form for young children with neuromuscular diseases. Arch Phys Med Rehabil 94(11):2218–2226PubMedCrossRef
66.
Zurück zum Zitat Emery N, Strachan K, Kulshrestha R, Kuiper JH, Willis T (2022) Evaluating the feasibility and reliability of remotely delivering and scoring the North Star ambulatory assessment in ambulant patients with duchenne muscular dystrophy. Children (Basel) 9(5):728PubMed Emery N, Strachan K, Kulshrestha R, Kuiper JH, Willis T (2022) Evaluating the feasibility and reliability of remotely delivering and scoring the North Star ambulatory assessment in ambulant patients with duchenne muscular dystrophy. Children (Basel) 9(5):728PubMed
67.
Zurück zum Zitat James MK, Alfano LN, Muni-Lofra R, Reash NF, Sodhi J, Iammarino MA, Moat D, Shannon K, McCallum M, Richardson M, Eagle M, Straub V, Marini-Bettolo C, Lowes LP, Mayhew AG (2022) Validation of the North star assessment for limb-girdle type muscular dystrophies. Phys Ther 102(10):pzac113PubMedPubMedCentralCrossRef James MK, Alfano LN, Muni-Lofra R, Reash NF, Sodhi J, Iammarino MA, Moat D, Shannon K, McCallum M, Richardson M, Eagle M, Straub V, Marini-Bettolo C, Lowes LP, Mayhew AG (2022) Validation of the North star assessment for limb-girdle type muscular dystrophies. Phys Ther 102(10):pzac113PubMedPubMedCentralCrossRef
68.
Zurück zum Zitat Boulay C, Finidori G (2015) Aspects fonctionnels et orthopédiques des dystrophinopathies [Functional and orthopaedic aspects of dystrophinopathies]. Arch Pediatr 22(12 Suppl 1):12S42-12S50PubMedCrossRef Boulay C, Finidori G (2015) Aspects fonctionnels et orthopédiques des dystrophinopathies [Functional and orthopaedic aspects of dystrophinopathies]. Arch Pediatr 22(12 Suppl 1):12S42-12S50PubMedCrossRef
69.
Zurück zum Zitat Lanza G, Pino M, Fisicaro F, Vagli C, Cantone M, Pennisi M, Bella R, Bellomo M (2020) Motor activity and Becker’s muscular dystrophy: lights and shadows. Phys Sportsmed 48(2):151–160PubMedCrossRef Lanza G, Pino M, Fisicaro F, Vagli C, Cantone M, Pennisi M, Bella R, Bellomo M (2020) Motor activity and Becker’s muscular dystrophy: lights and shadows. Phys Sportsmed 48(2):151–160PubMedCrossRef
70.
Zurück zum Zitat Alemdaroğlu I, Karaduman A, Yilmaz ÖT, Topaloğlu H (2015) Different types of upper extremity exercise training in Duchenne muscular dystrophy: effects on functional performance, strength, endurance, and ambulation. Muscle Nerve 51(5):697–705PubMedCrossRef Alemdaroğlu I, Karaduman A, Yilmaz ÖT, Topaloğlu H (2015) Different types of upper extremity exercise training in Duchenne muscular dystrophy: effects on functional performance, strength, endurance, and ambulation. Muscle Nerve 51(5):697–705PubMedCrossRef
71.
72.
Zurück zum Zitat Spitzer RL, Kroenke K, Williams JB, Löwe B (2006) A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med 166(10):1092–1097PubMedCrossRef Spitzer RL, Kroenke K, Williams JB, Löwe B (2006) A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med 166(10):1092–1097PubMedCrossRef
73.
Zurück zum Zitat Dany A, Rapin A, Lavrard B, Saoût V, Réveillère C, Bassez G, Tiffreau V, Péréon Y, Sacconi S, Eymard B, Dramé M, Jolly D, Novella JL, Hardouin JB, Boyer FC (2017) The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French version. Muscle Nerve 56(6):1085–1091PubMedCrossRef Dany A, Rapin A, Lavrard B, Saoût V, Réveillère C, Bassez G, Tiffreau V, Péréon Y, Sacconi S, Eymard B, Dramé M, Jolly D, Novella JL, Hardouin JB, Boyer FC (2017) The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French version. Muscle Nerve 56(6):1085–1091PubMedCrossRef
74.
Zurück zum Zitat Bushby K, Muntoni F, Bourke JP (2003) 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands. Neuromuscul Disord 13:166–72 Bushby K, Muntoni F, Bourke JP (2003) 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands. Neuromuscul Disord 13:166–72
75.
Zurück zum Zitat Nigro G, Comi LI, Politano L et al (1995) Evaluation of the cardiomyopathy in Becker muscular dystrophy. Muscle Nerve 18:283–291PubMedCrossRef Nigro G, Comi LI, Politano L et al (1995) Evaluation of the cardiomyopathy in Becker muscular dystrophy. Muscle Nerve 18:283–291PubMedCrossRef
76.
Zurück zum Zitat McDonagh TA, Metra M, Adamo M, Gardner RS, Baumbach A, Böhm M, Burri H, Butler J, Čelutkienė J, Chioncel O, Cleland JGF, Coats AJS, Crespo-Leiro MG, Farmakis D, Gilard M, Heymans S, Hoes AW, Jaarsma T, Jankowska EA, Lainscak M, Lam CSP, Lyon AR, McMurray JJV, Mebazaa A, Mindham R, Muneretto C, Piepoli MF, Price S, Rosano GMC, Ruschitzka F, Skibelund AK, ESC Scientific Document Group (2022) 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: developed by the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC) With the special contribution of the Heart Failure Association (HFA) of the ESC. Rev Esp Cardiol (Engl Ed) 75(6):523 (English, Spanish)PubMed McDonagh TA, Metra M, Adamo M, Gardner RS, Baumbach A, Böhm M, Burri H, Butler J, Čelutkienė J, Chioncel O, Cleland JGF, Coats AJS, Crespo-Leiro MG, Farmakis D, Gilard M, Heymans S, Hoes AW, Jaarsma T, Jankowska EA, Lainscak M, Lam CSP, Lyon AR, McMurray JJV, Mebazaa A, Mindham R, Muneretto C, Piepoli MF, Price S, Rosano GMC, Ruschitzka F, Skibelund AK, ESC Scientific Document Group (2022) 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: developed by the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC) With the special contribution of the Heart Failure Association (HFA) of the ESC. Rev Esp Cardiol (Engl Ed) 75(6):523 (English, Spanish)PubMed
77.
Zurück zum Zitat Quinlivan R, Ball J, Dunckley M, Thomas DJ, Flinter F, Morgan-Hughes J (1995) Becker muscular dystrophy presenting with complete heart block in the sixth decade. J Neurol 242(6):398–400PubMedCrossRef Quinlivan R, Ball J, Dunckley M, Thomas DJ, Flinter F, Morgan-Hughes J (1995) Becker muscular dystrophy presenting with complete heart block in the sixth decade. J Neurol 242(6):398–400PubMedCrossRef
78.
Zurück zum Zitat Nolan MA, Jones ODH, Pedersen RL et al (2003) Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophies. Neuromuscul Disord 13:129–132PubMedCrossRef Nolan MA, Jones ODH, Pedersen RL et al (2003) Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophies. Neuromuscul Disord 13:129–132PubMedCrossRef
79.
Zurück zum Zitat Politano L, Nigro V, Nigro G et al (1996) Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies. JAMA 275:1335–1338PubMedCrossRef Politano L, Nigro V, Nigro G et al (1996) Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies. JAMA 275:1335–1338PubMedCrossRef
80.
Zurück zum Zitat Rahbek J, Steffensen BF, Bushby K et al (2015) 206th ENMC International Workshop: care for a novel group of patients—adults with Duchenne muscular dystrophy Naarden, The Netherlands, 23–25 May 2014. Neuromuscul Disord 25:727–738PubMedCrossRef Rahbek J, Steffensen BF, Bushby K et al (2015) 206th ENMC International Workshop: care for a novel group of patients—adults with Duchenne muscular dystrophy Naarden, The Netherlands, 23–25 May 2014. Neuromuscul Disord 25:727–738PubMedCrossRef
81.
Zurück zum Zitat Stalens C, Motté L, Béhin A, Ben Yaou R, Leturcq F, Bassez G, Laforêt P, Fontaine B, Ederhy S, Masingue M, Saadi M, Louis SL, Berber N, Stojkovic T, Duboc D, Wahbi K (2021) Improved cardiac outcomes by early treatment with angiotensin-converting enzyme inhibitors in becker muscular dystrophy. J Neuromuscul Dis 8(4):495–502PubMedPubMedCentralCrossRef Stalens C, Motté L, Béhin A, Ben Yaou R, Leturcq F, Bassez G, Laforêt P, Fontaine B, Ederhy S, Masingue M, Saadi M, Louis SL, Berber N, Stojkovic T, Duboc D, Wahbi K (2021) Improved cardiac outcomes by early treatment with angiotensin-converting enzyme inhibitors in becker muscular dystrophy. J Neuromuscul Dis 8(4):495–502PubMedPubMedCentralCrossRef
82.
Zurück zum Zitat Viollet L, Thrush PT, Flanigan KM et al (2012) Effects of angiotensin-converting enzyme inhibitors and/or beta blockers on the cardiomyopathy in Duchenne muscular dystrophy. Am J Cardio 110:98–102CrossRef Viollet L, Thrush PT, Flanigan KM et al (2012) Effects of angiotensin-converting enzyme inhibitors and/or beta blockers on the cardiomyopathy in Duchenne muscular dystrophy. Am J Cardio 110:98–102CrossRef
83.
Zurück zum Zitat American Academy of Pediatrics Section on Cardiology and Cardiac Surgery (2005) Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy. Pediatrics 116:1569–1573CrossRef American Academy of Pediatrics Section on Cardiology and Cardiac Surgery (2005) Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy. Pediatrics 116:1569–1573CrossRef
85.
Zurück zum Zitat Yuko Nakamura et col. Brain & Development (2018) Identification of sleep hypoventilation in young individuals with Becker muscular dystrophy: a pilot study Yuko Nakamura et col. Brain & Development (2018) Identification of sleep hypoventilation in young individuals with Becker muscular dystrophy: a pilot study
86.
Zurück zum Zitat Finder JD (2009) A 2009 perspective on the 2004 American Thoracic Society statement, “respiratory care of the patient with Duchenne muscular dystrophy.” Pediatrics 123:S239–S241PubMedCrossRef Finder JD (2009) A 2009 perspective on the 2004 American Thoracic Society statement, “respiratory care of the patient with Duchenne muscular dystrophy.” Pediatrics 123:S239–S241PubMedCrossRef
87.
Zurück zum Zitat Michelle C, Hui-Leng T, Andrew B, Mark R, Anita KS (2015) Long term non-invasive ventilation in children: impact on survival and transition to adult care. PLoS One 10(5):e0125839 Michelle C, Hui-Leng T, Andrew B, Mark R, Anita KS (2015) Long term non-invasive ventilation in children: impact on survival and transition to adult care. PLoS One 10(5):e0125839
88.
Zurück zum Zitat Annane D, Orlikowski D, Chevret S (2014) Cochrane Database of Systematic Reviews 2014, Issue 12. Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders (Review) Annane D, Orlikowski D, Chevret S (2014) Cochrane Database of Systematic Reviews 2014, Issue 12. Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders (Review)
90.
Zurück zum Zitat Elverson J, Evans H, Dewhurst F (2023) Palliation, end of life care and ventilation withdrawal in neuromuscular disorders. Chron Respir Dis 20:14799731231175912PubMedPubMedCentralCrossRef Elverson J, Evans H, Dewhurst F (2023) Palliation, end of life care and ventilation withdrawal in neuromuscular disorders. Chron Respir Dis 20:14799731231175912PubMedPubMedCentralCrossRef
91.
Zurück zum Zitat Yamada Y, Kawakami M, Wada A, Otsuka T, Muraoka K, Liu M (2018) A comparison of swallowing dysfunction in Becker muscular dystrophy and Duchenne muscular dystrophy. Disabil Rehabil 40(12):1421–1425PubMedCrossRef Yamada Y, Kawakami M, Wada A, Otsuka T, Muraoka K, Liu M (2018) A comparison of swallowing dysfunction in Becker muscular dystrophy and Duchenne muscular dystrophy. Disabil Rehabil 40(12):1421–1425PubMedCrossRef
92.
Zurück zum Zitat Okan M, Alper E, Cil E, Eralp O, Ağir H (1997) Gastric emptying time in children with progressive muscular dystrophy. Turk J Pediatr 39(1):69–74PubMed Okan M, Alper E, Cil E, Eralp O, Ağir H (1997) Gastric emptying time in children with progressive muscular dystrophy. Turk J Pediatr 39(1):69–74PubMed
93.
Zurück zum Zitat Morse CI, Higham K, Bostock EL, Jacques MF (2020) Urinary incontinence in men with Duchenne and Becker muscular dystrophy. PLoS One 15(5):e0233527PubMedPubMedCentralCrossRef Morse CI, Higham K, Bostock EL, Jacques MF (2020) Urinary incontinence in men with Duchenne and Becker muscular dystrophy. PLoS One 15(5):e0233527PubMedPubMedCentralCrossRef
94.
Zurück zum Zitat Bertrand LA, Askeland EJ, Mathews KD, Erickson BA, Cooper CS (2016) Prevalence and bother of patient-reported lower urinary tract symptoms in the muscular dystrophies. J Pediatr Urol 12(6):398.e1-398.e4PubMedCrossRef Bertrand LA, Askeland EJ, Mathews KD, Erickson BA, Cooper CS (2016) Prevalence and bother of patient-reported lower urinary tract symptoms in the muscular dystrophies. J Pediatr Urol 12(6):398.e1-398.e4PubMedCrossRef
95.
Zurück zum Zitat Mahoney FI, Barthel DW (1965) Functional evaluation: the Barthel index. Md State Med J 14:61–65PubMed Mahoney FI, Barthel DW (1965) Functional evaluation: the Barthel index. Md State Med J 14:61–65PubMed
96.
Zurück zum Zitat Avery K, Donovan J, Peters TJ, Shaw C, Gotoh M, Abrams P (2004) ICIQ: a brief and robust measure for evaluating the symptoms and impact of urinary incontinence. Neurourol Urodyn Off J Int Cont Soc 23(4):322–330CrossRef Avery K, Donovan J, Peters TJ, Shaw C, Gotoh M, Abrams P (2004) ICIQ: a brief and robust measure for evaluating the symptoms and impact of urinary incontinence. Neurourol Urodyn Off J Int Cont Soc 23(4):322–330CrossRef
97.
Zurück zum Zitat Houwen-van Opstal SLS, Rodwell L, Bot D, Daalmeyer A, Willemsen MAAP, Niks EH, de Groot IJM (2022) BMI-z scores of boys with Duchenne muscular dystrophy already begin to increase before losing ambulation: a longitudinal exploration of BMI, corticosteroids and caloric intake. Neuromuscul Disord 32(3):236–244PubMedCrossRef Houwen-van Opstal SLS, Rodwell L, Bot D, Daalmeyer A, Willemsen MAAP, Niks EH, de Groot IJM (2022) BMI-z scores of boys with Duchenne muscular dystrophy already begin to increase before losing ambulation: a longitudinal exploration of BMI, corticosteroids and caloric intake. Neuromuscul Disord 32(3):236–244PubMedCrossRef
98.
Zurück zum Zitat Coubes C (2015) Conseil génétique dans les dystrophinopathies. Arch Pediatr 22(12 Suppl 1):12S12-12S17PubMedCrossRef Coubes C (2015) Conseil génétique dans les dystrophinopathies. Arch Pediatr 22(12 Suppl 1):12S12-12S17PubMedCrossRef
99.
Zurück zum Zitat Segura LG, Lorenz JD, Weingarten TN, Scavonetto F, Bojaniƒá K, Selcen D, Sprung J (2013) Anesthesia and Duchenne or Becker muscular dystrophy: review of 117 anesthetic exposures. Paediatr Anaesth 23(9):855–864PubMedCrossRef Segura LG, Lorenz JD, Weingarten TN, Scavonetto F, Bojaniƒá K, Selcen D, Sprung J (2013) Anesthesia and Duchenne or Becker muscular dystrophy: review of 117 anesthetic exposures. Paediatr Anaesth 23(9):855–864PubMedCrossRef
100.
Zurück zum Zitat Bush A, Dubowitz V (1991) Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy. Neuromuscul Disord 1:201–204PubMedCrossRef Bush A, Dubowitz V (1991) Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy. Neuromuscul Disord 1:201–204PubMedCrossRef
101.
Zurück zum Zitat Cripe LH, Tobias JD (2013) Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr Anaesth 23(9):777–784PubMedCrossRef Cripe LH, Tobias JD (2013) Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr Anaesth 23(9):777–784PubMedCrossRef
102.
Zurück zum Zitat van den Bersselaar LR, Heytens L, Silva HCA, Reimann J, Tasca G, Díaz-Cambronero Ó, Løkken N, Hellblom A, Hopkins PM, Rueffert H, Bastian B, Vilchez JJ, Gillies R, Johannsen S, Veyckemans F, Muenster T, Klein A, Litman R, Jungbluth H, Riazi S, Voermans NC, Snoeck MMJ (2022) European Neuromuscular Centre consensus statement on anaesthesia in patients with neuromuscular disorders. Eur J Neurol 29(12):3486–3507PubMedPubMedCentralCrossRef van den Bersselaar LR, Heytens L, Silva HCA, Reimann J, Tasca G, Díaz-Cambronero Ó, Løkken N, Hellblom A, Hopkins PM, Rueffert H, Bastian B, Vilchez JJ, Gillies R, Johannsen S, Veyckemans F, Muenster T, Klein A, Litman R, Jungbluth H, Riazi S, Voermans NC, Snoeck MMJ (2022) European Neuromuscular Centre consensus statement on anaesthesia in patients with neuromuscular disorders. Eur J Neurol 29(12):3486–3507PubMedPubMedCentralCrossRef
103.
Zurück zum Zitat Esposito S, Bruno C, Berardinelli A, Filosto M, Mongini T, Morandi L, Musumeci O, Pegoraro E, Siciliano G, Tonin P, Marrosu G, Minetti C, Servida M, Fiorillo C, Conforti G, Scapolan S, Ansaldi F, Vianello A, Castaldi S, Principi N, Toscano A, Moggio M (2014) Vaccination recommendations for patients with neuromuscular disease. Vaccine 32(45):5893–5900PubMedCrossRef Esposito S, Bruno C, Berardinelli A, Filosto M, Mongini T, Morandi L, Musumeci O, Pegoraro E, Siciliano G, Tonin P, Marrosu G, Minetti C, Servida M, Fiorillo C, Conforti G, Scapolan S, Ansaldi F, Vianello A, Castaldi S, Principi N, Toscano A, Moggio M (2014) Vaccination recommendations for patients with neuromuscular disease. Vaccine 32(45):5893–5900PubMedCrossRef
104.
Zurück zum Zitat Dowell D, Ragan KR, Jones CM, Baldwin GT, Chou R (2022) CDC clinical practice guideline for prescribing opioids for pain—United States, 2022. MMWR Recomm Rep 71(3):1–95PubMedPubMedCentralCrossRef Dowell D, Ragan KR, Jones CM, Baldwin GT, Chou R (2022) CDC clinical practice guideline for prescribing opioids for pain—United States, 2022. MMWR Recomm Rep 71(3):1–95PubMedPubMedCentralCrossRef
106.
Zurück zum Zitat Zagorda B, Camdessanché JP, Féasson L (2021) Pregnancy and myopathies: reciprocal impacts between pregnancy, delivery, and myopathies and their treatments. A clinical review. Rev Neurol (Paris) 177(3):225–234PubMedCrossRef Zagorda B, Camdessanché JP, Féasson L (2021) Pregnancy and myopathies: reciprocal impacts between pregnancy, delivery, and myopathies and their treatments. A clinical review. Rev Neurol (Paris) 177(3):225–234PubMedCrossRef
Metadaten
Titel
Diagnosis and management of Becker muscular dystrophy: the French guidelines
verfasst von
Armelle Magot
Karim Wahbi
France Leturcq
Sandrine Jaffre
Yann Péréon
Guilhem Sole
The French BMD working group
Publikationsdatum
09.07.2023
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Neurology / Ausgabe 10/2023
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-023-11837-5

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