A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report

About 1–3% of females with unexplained intellectual disability (ID) carry de novo pathogenic variants in the X-linked DDX3X gene (Xp11.4) [1]. Up to about 300 cases have been identified [2], both females with X-linked dominant inheritance, and very few males showing an X-linked recessive pattern of inheritance [1].

To date, all reported pathogenic DDX3X variants identified in affected females are de novo loss of function, leading to haploinsufficiency and, probably, to embryonic lethality in males. Most of DDX3X mutations reported in males are maternally inherited missense variants. In these families, males showed borderline to severe ID and carrier females were unaffected and expressed a DDX3X protein retaining a partial functionality [1]. Several hypotheses have been evaluated to explain the gender-specific pathogenicity, including a skewing X-inactivation pattern, but no definitive conclusions have been drawn. Kellaris et al. [3] proposed that hypomorphic DDX3X variants may be viable in hemizygous males and do not cause clinical phenotype in female carriers. However, few de novo DDX3X mutations have been identified in males [4]. Although these male patients share many of the clinical features with affected females, some distinct clinical phenotypes can depend on the gender of the patient and on the pathogenicity of the variant. These findings suggest that the DDX3X gene exerts dose-dependent and gender-specific effects in normal development and disease [5]. Indeed, Snijders Blok et al. [1] reported a family with recurrent miscarriages of unknown gender and a male viable pregnancy, terminated after the identification of severe congenital anomalies by ultrasound imaging. By whole exome sequencing (WES) a missense mutation in the DDX3X gene was detected in the fetus, suggesting a potential germline mosaicism in the mother.

The DDX3X gene encodes a DEAD-box ATP-dependent RNA-helicase broadly implicated in gene expression through regulation of mRNA metabolism [6]. It acts as a translational regulator of target mRNAs with highly structured 5′ untranslated regions (UTRs) and it is involved in repeat-associated non-AUG translation [7]. DDX3X also takes part in stress response and stress granule assembly, innate immune signaling, mitotic chromosome segregation and it can also exert a role in tumorigenesis [8]. In addition, it is thought to be an essential factor in the RNA-interference pathway [9], and it is a key regulator of the Wnt/β-catenin pathway [10].

Despite the ubiquitous expression of the DDX3X protein, high expression levels are detected in all the cortical layers of the embryonic brain, consistent with its crucial role in cortical development during neurogenesis [10] and, as a consequence, DDX3X mutations are reported to impact on neuronal function [4]. In particular, defective neurite outgrowth and neural progenitor differentiation/migration could account for brain malformations and the consequent characteristic clinical phenotypes of the DDX3X syndrome [5].

Here, we report a 10-year-old girl with delayed psychomotor development, delayed myelination, bilateral frontal PMG and thin body and splenium of the corpus callosum. WES allowed the identification of the novel de novo DDX3X mutation c.625C > G (p.His209Asp), leading to a diagnosis of DDX3X syndrome and expanding the number of DDX3X pathogenic variants and their associated phenotypic spectrum.

The proband was referred to our laboratory by the pediatric geneticists of our Institution, Fondazione IRCCS Ca′ Granda Ospedale Policlinico (Milan). Appropriate written informed consent was obtained from all family members.

Patient II-3 (Fig. 1A), who is currently 10 years old, is the third-born of healthy parents with a doubtful distant consanguinity (beyond the second generation). The two older siblings (II-1 and II-2, of 16 and 14 years old respectively) are both healthy. Between the first and second pregnancy three miscarriages of unknown gender occurred, but no additional information is available. The family history is negative for genetic conditions.

The patient was born at 38 + 5 gestational weeks, after a normal pregnancy, characterized by regular growth, morphology and fetal movements. She was born by cesarean delivery scheduled for previous cesarean section.

Clinical signs are reported in Table 1. At birth, the child was 2740 g (25th centile), 49 cm long (50th centile), presented an occipitofrontal circumference of 34 cm (50th centile) and an Apgar score of 10–10. Absence of skin adnexa (eyelashes, eyebrows and nails) and difficult scarring of the umbilical stump are referred. In addition, a bilateral II-III toe syndactyly and a small left preauricular tag were evident. Ultrasounds revealed normal abdominal and cerebral morphology.

In the first months of life, a severe gastro-esophageal reflux with initial weight loss and sleep disturbance was reported, which improved after the introduction of proton-pump inhibitors therapy.

Growth was regular, but psychomotor development was severely delayed, with independent walking and babbling acquired towards 6 years of age.

Evaluation at 6 years old revealed the following cranio-facial dysmorphisms: brachycephaly and a flattened-triangular-asymmetrical face characterized by micrognathia, mild hypertelorism, wide and prominent nose, short philtrum, thin lips and macroglossia. She also presented a slight facial grimacing, large and anteverted ears and small left ear tag. Growth parameters were normal, with a weight of 16.5 kg (10-25th centiles), a height of 111 cm (50-75th centile), head circumference of 50.5 cm (25-50th centile).

Brain MRI performed at 6 months of age showed delayed myelination (improved at the second MRI performed at 2 years old), bilateral frontal PMG and thin body and splenium of the corpus callosum (Fig. 1B). Electroencephalogram (EEG) showed sharp-wave anomalies on the rear right regions. She also presents hyperopia and divergent strabismus.

Karyotype, aCGH and mutational analysis of the ADGRG1 gene (associated to bilateral frontoparietal PMG resulted normal. An NGS panel for Rett syndrome (including the MECP2, CDKL5, FOXG1, MEF2C, SCN1A, UBE3A, PCDH19, STXBP1 genes) was also performed, and no pathogenic variants were identified.

Since no other clinical suspicions were hypothesized, the proband and her parents underwent WES on DNA extracted from peripheral blood leukocytes. Trio WES and variants interpretation according to the pedigree and the clinical features allowed the identification of the novel missense variant c.625C > G (p.His209Asp) in exon 7 of the DDX3X gene. No other candidate variants were found, and the identified variant was confirmed by Sanger sequencing. The absence of the mutation in the healthy mother confirmed the hypothesis of a de novo inheritance (Fig. 1C). However, considering the occurrence of three miscarriages between the first and the second pregnancy, we cannot exclude the possibility that also the aborted fetuses could have carried the c.625C > G mutation as a consequence of a possible germline mosaicism in the mother.

The identified DDX3X variant is neither reported in ClinVar nor in HGMD Professional 2020.1. To determine the impact of this amino acid substitution, the pathogenic score was evaluated by thirteen different in-silico predictors, and it was predicted to be damaging by nine of them (Supplementary Table 1). This score is consistent with the amino acid substitution from a positively charged histidine to a negatively charged aspartic acid, in a highly conserved residue.

WES analysis in a 10-year-old girl with delayed psychomotor development, characteristic facial dysmorphisms and brain malformations, including delayed myelination, bilateral frontal PMG and thin body and splenium of the corpus callosum, allowed the identification of the novel missense variant c.625C > G (p.His209Asp) in exon 7 of the DDX3X gene, suggesting a diagnosis of DDX3X syndrome. The absence of the mutation in the healthy mother confirmed the hypothesis of a de novo inheritance (Fig. 1C), as reported for all DDX3X mutations found in females [1]. However, considering the occurrence of three miscarriages between the first and the second pregnancy, we cannot exclude the possibility that also the aborted fetuses could have carried the c.625C > G mutation as a consequence of a possible germline mosaicism in the mother. This is consistent with the association of DDX3X mutations to miscarriage recurrence and aborted male fetuses [1]. However, the unavailability of information on the aborted fetuses and the impossibility to assess the presence of the germline mosaicism in the mother prevents us to confirm this hypothesis.

The novel c.625C > G variant involves the amino acidic position 209, which maps 2 bp upstream the helicase ATP binding domain (Fig. 2). Most reported DDX3X mutations map within the two helicase domains impairing the protein helicase activity, with a dominant negative mechanism [10]. The novel His209Asp variant is close to the Val206Met, already reported in a patient with the DDX3X syndrome [10]. Despite no functional tests have been performed to confirm the pathogenic effect of this novel mutation, according to in silico predictions and literature data on the close Val206Met and other missense mutations that fall within or in proximity of the DDX3X helicase domain [10], we hypothesize that also the His209Asp variant leads to an impaired helicase activity. Deficient DDX3X helicase activity results in the enzyme inability to release the bound RNA after ATP hydrolysis and the altered translation of DDX3X-dependent targets, in particular mRNAs containing highly structured 5′ UTRs and/or high GC content [12]. This leads to the sequestration of RNAs and RNA binding proteins, and the formation of aberrant ribonucleoprotein (RNP) granules containing newly synthetized proteins and/or stalled polysomes [10]. The defective translation of DDX3X-target transcripts has been proposed to lead to impaired neurogenesis, likely affecting embryonic cortical development [10]. This mechanism may also account for the more severe phenotypes associated with missense mutations, compared to nonsense and frameshift (presumed loss of function) lesions, that affect translation of some targets but do not induce granule formation, resulting in a less severe clinical presentation [10]. This pathomechanism may also apply to the His209Asp mutation here reported, as suggested, not only by the affected protein domain, but also by the PMG phenotype of the proband herein presented.

According to the recent studies on genotype-phenotype correlations in the DDX3X syndrome and underlying pathogenetic mechanisms [10], patients with severe cerebral defects, including complete or partial absence of the corpus callosum and PMG (frequently associated to microcephaly), presented missense mutations or single amino acid deletion hotspot mutations, including the nearby Val206Met (Fig. 2). These mutations are also associated to more complex clinical presentations, including epilepsy, autism spectrum disorder, severe intellectual disability, and cardiovascular anomalies, not present in patients without PMG [10]. This evidence thus suggests that these variants are likely to lead to a more severe dominant negative phenotype, while loss of function mutations are associated to a milder spectrum of clinical traits with no signs of PMG. Despite the proband herein described presents with PMG, she does not show other clinical traits reported in most severe cases of DDX3X syndrome, such as microcephaly, congenital cardiac defects and epilepsy (she only presents EEG anomalies) (Table 1). In addition, she shows reduced subcutaneous fat, already reported in two other patients DDX3X syndrome patients [11], and she is the first female patient presenting with brachycephaly (which has so far been described only in few males [1]) (Table 1). She also has macroglossia, an additional clinical sign that has never been associated with the DDX3X syndrome before (Table 1).

This case report emphasizes the clinical utility of WES in ending the diagnostic odyssey of individuals with unexplained ID.