Background

WDR62 plays an important role in cerebral cortical development. It is also one of the main pathogenic genes (only after ASPM) for autosomal recessive primary microcephaly 2 (MCPH2), which is a neurodevelopmental disorder characterized by microcephaly presenting at birth and nonprogressive mental retardation [1,2,3,4]. West syndrome is a severe epilepsy syndrome composed of the triad of spasms, interictal hypsarrhythmia shown in electroencephalogram(EEG) and mental retardation. Up to now, West syndrome has been rarely reported to be related with WDR62 mutation. In this study, we reported a boy with compound heterozygous WDR62 mutations, diagnosed as MCPH2 and West syndrome. The informed consent of the parents and the approval of the ethics committee (SZCH [Article] 2019 /002) were obtained.

Case presentation

The child patient, male, is the first child of a healthy Chinese genetically unrelated couple. He was born at full term following an uneventful vaginal delivery with length 49 cm (SD 0.47), weight 3.2 kg (SD 0.3), and head circumference 32 cm (SD 2). He reached his normal milestone at the age of 2 months. He was able to hold head, track light or sound, and laugh initiatively. But the parents noticed that he lost the ability to hold head steadily and couldn't track light or sound by the age of 4 months.

At the age of 4 months, the boy was hospitalized because of recurrent seizures including focal seizure and epileptic spasm. His body weight and head circumference were 6.5 kg (SD 0.68) and 38.5 cm (SD 2.6) respectively. On physical examination, one cafe-au-lait macule (8×4 cm2) on the left thigh and one hemangioma (about 2×2 cm2) on the neck were noted. Muscle tone was slightly lower than normal in all extremities.

Head magnetic resonance imaging (MRI) at 3 months and 13 days (Fig. 1) showed neuronal migration disorder and multiple gyrus malformations. Shallow sulci, widened gyri and thickened bilateral cerebral cortex were noticed in both cerebral hemispheres, and polymicrogyria in some areas. The first EEG was performed at 3 months and 12 days. It showed many sharp waves during wakefulness and sleep, which were asymmetrical and predominant at the posterior area, sometimes simultaneously appeared in the central and mid-temporal areas. The second EEG was performed at 4 months and 20 days (Fig. 2), which indicated hypsarrhythmia during sleep and wakefulness. Clinical epileptic spasms were identified during this EEG recording.

Fig. 1
figure 1

Brain magnetic resonance imaging (MRI) of the patient. Shallow sulci, widened gyri and thickened bilateral cerebral cortex were noticed in bilateral hemispheres, and polymicrogyria in some areas. (the arrow) a: Axial T1; b: Axial T2; c: Coronal T2 FLAIR; d: Axial T2 FLAIR

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Fig. 2
figure 2

The second electroencephalogram (EEG) of the patient. a: interictal EEG, periodical hypsarrhythmia, diffuse irregular medium-high amplitude slow waves mixed with a large number of disorderly multifocal spikes and sharp waves, which were asymmetrical, synchronous/asynchronous. b: ictal EEG, epileptic spasm occurred with irregular high amplitude slow waves followed by short fast activities during the EEG recording

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The trios whole exome sequencing (WES) [5] of the family were performed at 4 months and 18 days (Running Gene Inc). Two heterozygous variants were identified in the WDR62: c.1535G > A, p.R512Q, inherited from the mother; c.2618dupT, p.K874Qfs*40, inherited from the father (Fig. 3). These two variants had not been reported in literatures, and the frequency in the healthy population was very low. The p.K874Qfs*40 is a frameshift mutation that leads to the early termination of protein translation and may have a great effect on protein function. American College of Medical Genetics and Genomics (ACMG) variation rating is likely pathogenic. The p.R512Q is a missense mutation, and the amino acid is well conservative, which may affect the function of protein (Mutation Taster: disease causing, 0.999; PolyPhen-2: probably damaging, 0.998; SIFT: damaging, 0.037). ACMG variation rating is variation uncertain significance (VUS). The phenotype of the child was consistent with the phenotype and genetic pattern of WDR62 mutation that had been reported, so the WDR62 compound heterozygous mutation in our study were considered to be pathogenic.

Fig. 3
figure 3

Sanger sequencing of WDR62 variants of the child patient and his parents. a: The heterozygous mutation c.1535G > A of WDR62 was found in the chr19:36574128 of the child and his mother, but no variant was found at the same locus of his father (circled part); b: The heterozygous mutation c.2618dupT of WDR62 was found in the chr19:36590397 of the child and his father, but no variant was found at the same locus of the mother (circled part)

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The patient was administered sodium valproate (18.4 mg/kg/d) and nitrazepam (from 0.48 mg/kg/d to 1.44 mg/kg/d) at the early stages of the disease, whereas the seizures were poorly controlled. After 2 weeks of intramuscular adrenocorticotropic hormone (ACTH) therapy (1 U/ kg, twice daily for 1 week then increase to 2 U/kg, twice daily for 1 week), the patient was administered with oral prednisolone (2 mg/kg/d), and the seizure frequency was slightly decreased from 3 to 5 series/d to 2–4 series/d. After the administration of levetiracetam (20 mg/kg/d), topiramate (1.92 mg/kg/d) and vigabatrin (38.46 mg/kg/d), the patient still had epileptic spasms, and had a new seizure type manifested as follows: clenched fists with both hands, upper limbs tonic, occurred in series, lasted 2–7 min, 6–7 series/d, which were considered as tonic-spasms. Ketogenic diet was tried and the frequency of seizure was lowered slightly to 4–5 series/d transiently. Lamotrigine (0.67 mg/kg/d) was administered, but withdrawn soon because of transient skin rash and exacerbation of seizure frequency. To relieve the seizure burden, corpus callosotomy was recommended to the parents. However, they refused this operation in consideration of the young age and the possible complications.

Discussion

WDR62 is located in chromosome 19q13.12, composing of 32 exons, encodes 1523 amino acids, and the protein contains multiple WD40 repeats [6, 7]. Mutations in the WDR62 can cause severe cerebral cortical abnormalities, including microcephaly, cerebral gyrus hypertrophy with cortical thickening and dysplasia of corpus callosum [6, 8, 9], all inherited in an autosomal recessive. A number of neurobehavioral abnormalities have been reported, including psychomotor developmental delay, seizure, aggression and irritability [9,10,11]. In addition, some case reports claimed that WDR62 mutation can also cause skin changes [12].

Taking “WDR62” and “West syndrome”, “WDR62” and “infantile spasms” as the keywords to search on PubMed, we found only one publication by Nardello R et al. in 2018, which reported WDR62 and GPR56 variants in a patient with MCPH2. Literatures have reported variable and unstable frequency and severity of seizures in children with WDR62 variant. However, in this case, the severity of seizure and its effect on overall mental function were the major phenotype. This suggested that WDR62 and other mutated genes may work together to regulate the severity of genetic phenotype [13]. Therefore, we cautiously put forward the hypothesis that the combined effect of c.1535G > A and c.2618dupT of WDR62 variants may lead to abnormal change of brain structure in this child, which further lead to refractory epilepsy and psychomotor retardation.

C-terminal of WDR62 has regulatory function, and N-terminal is necessary for spindle microtubule binding. WDR62 could regulate mitotic spindle orientation, centrosome integrity and progression via Aurora kinase and JNK mitogen-activated protein kinase (MAPK) signaling pathway [7, 14]. In the early stages of the cell cycle, WDR62 is located at the poles of mitotic spindle [12]. Immunocytochemistry studies have shown that WDR62 exhibits cytoplasmic distribution during the intermitotic phase, but accumulates in large quantities at the spindle poles during mitosis. The reduced proteins caused by WDR62 mutation fail to locate at the poles of the mitotic spindle, resulting in the destruction of the asymmetric inheritance of the centrosome and the abnormal development of brain structure in children. In 2015, Kodani A et al. showed that four microcephaly-related proteins, CDK5RAP2, CEP152, WDR62 and CEP63, were co-located in the centrosome [15]. CDK2 is a kind of cell cycle-dependent kinases, which plays an important role in centrosome replication and cell cycle process, and its centrosome localization requires the interaction of microcephaly-associated proteins as well as their centromeric satellite proteins. The dysfunction of WDR62 can disrupt centrosome replication and stability [15]. In addition, several studies about pedigree-specific deletion of WDR62 revealed that WDR62 contributes to brain growth in neuroblastoma cells and peripheral glial cell lines. The loss of WDR62 in glial cell lines can increase the death risk of neural stem cells and significantly reduce the pool of neuroblastoma cells, thus damage the growth of brain. Therefore, the dysfunction of WDR62 in glial cells may also be one of the reasons for the abnormal development of brain structure [16].

West syndrome is an age-dependent disease [17], which may cause by non-specific damages occured at the critical point of brain ontogenesis. ACTH and vigabatrin are currently recommended as the first-line treatments for West syndrome [18, 19]. We believe that WDR62 missense mutation and frameshift mutation may lead to severe abnormal development of brain structure in this child, which is related to refractory West syndrome. Specific treatments for WDR62 variants have not been reported, though seizure was controlled by valproic acid, vigabatrin and carbamazepine in few patients. However, the clinical manifestations and treatment of refractory West syndrome caused by WDR62 variants have not been paid much attention. Ketogenic diet is effective and tolerated for West syndrome in some reports [20, 21], especially combined with vigabatrin [22]. Some adverse effects including hypertriglyceridemia, transient acidosis, poor sleep, and constipation have been reported during this diet [23, 24]. We also tried ketogenic diet in this case, otherwise, it didn’t show any significant advantage than other medicines. Corpus callosotomy is considered as a palliative surgery for drug-resistant epilepsy, which could improve the seizure outcome on some West syndrome [25, 26], especially epileptic spasms. We will try it if we get the consent from his parents.

Conclusion

In conclusion, due to the variants of WDR62 a phenotype including microcephaly, refractory West syndrome and psychomotor retardation was reported in this case. Further study is needed to explore the relationship between WDR62 variant and epileptic encephalopathy and the specific mechanism involved in the pathogenesis of MCPH2. Our report enriched the phenotypic and genotypic spectrum of MCPH2 and West syndrome, indicating that genetic investigation was valuable for children with refractory epilepsy and microcephaly, and will help to further guide early clinical intervention and individualized therapy.