Clinical features and genetic analysis of developmental and epileptic encephalopathy caused by biallelic variants of .

OBJECTIVE

To analyze the clinical features and genetic etiology of a patient with developmental and epileptic encephalopathy.

METHODS

The clinical information and peripheral blood of the patient and their family members were collected before the whole exome sequencing analysis was performed and Sanger sequencing was employed to verify the potential variant.

RESULTS

The patient presented with epilepsy and cerebral palsy with his parents, brother, and sister being all healthy. Whole exome sequencing analysis revealed that the child carried the paternal c.823del (p. R275Gfs31) heterozygous variant and the maternal c.2456del (p.V819Gfs190) heterozygous variant of the gene. Pedigree verification found that the elder brother and amniotic fluid of fetus in womb carried the paternal c.823del heterozygous variant, and the elder sister carried the maternal c.2456del heterozygous variant, which conformed to the law of autosomal recessive inheritance. Neither of these two variants has been reported in the literature and has not been included in the Genomic Mutation Frequency Database (gnomAD); according to the American Academy of Medical Genetics and Genomics Variation Grading Guidelines (ACMG), both variants are classified as pathogenic variants (PVS1+PM2-Supporting + PM3).

CONCLUSION

This study reported the first case of a child with neurodevelopmental disorder and epilepsy caused by a new compound heterozygous variant of the gene in China, clarified its genetic etiology, enriched the mutation spectrum and disease spectrum of gene, and provided a basis for prenatal diagnosis of the family.