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Am J Med Genet A ; 179(4): 645-649, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30680869

RESUMO

TBC1D24-related disorders are rare neurodevelopmental disorders that show a broad range of neuropsychiatric deficits and are mostly inherited in an autosomal recessive manner. Here we describe a case with early-onset epileptic encephalopathy, in whom exome sequencing detected a novel pathogenic homozygous c.442G>A, p.(Glu148Lys) variant in TBC1D24. She showed severe developmental delay, congenital sensorineural hearing loss and seizures, but the combination of a high dose phenobarbital and potassium bromide was very effective for the seizures. Sanger sequencing revealed that her mother was a heterozygous carrier of the TBC1D24 variant, but her father showed only wild-type alleles. Homozygosity mapping analysis using exome data showed loss of the heterozygosity region at 16p13.3-p13.13 encompassing TBC1D24. Genotyping analysis using rare variants within loss of the heterozygosity region indicated that the patient has a homozygous haplotype inherited from her mother, indicating maternal segmental uniparental isodisomy (UPiD). These data clearly show that exome sequencing is a powerful tool to perform comprehensive genetic analysis.


Assuntos
Proteínas Ativadoras de GTPase/genética , Homozigoto , Mutação , Espasmos Infantis/etiologia , Dissomia Uniparental/patologia , Exoma , Feminino , Humanos , Lactente , Prognóstico , Espasmos Infantis/patologia , Dissomia Uniparental/genética
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