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New variants in FLNA gene cause periventricular nodular heterotopia and epileptic seizure in three cases / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 626-630, 2021.
Artigo em Chinês | WPRIM | ID: wpr-888361
ABSTRACT
OBJECTIVE@#To explore the genetic bases of 3 patients with periventricular nodular heterotopia and epileptic seizure.@*METHODS@#The clinical data of three patients presenting with periventricular nodular ectopic with epileptic seizure were analyzed. Whole exome sequencing (WES) was performed on the patients, and Sanger sequencing was used to validate the suspected variants.@*RESULTS@#In three female patients, head MRI showed nodular gray matter ectopic in the bilateral ventricle. WES identified the heterozygous c.2720del T(p.Leu907Argfs*39) variant of FLNA gene in case 1 and her mother (case 2), and heterozygous c.1387_1390del GTGC(p.Val463Profs*34) of FLNA gene in case 3. According to the American College of Medical Genetics and Genomics standards and guidelines, the c.2720delT(p.Leu907Argfs*39) and c.1387_1390del GTGC (p.Val463Profs*34) variants of FLNA gene were predicted to be pathogenic (PVS1+PM2+PP1) and likely pathogenic(PVS1+PM2), respectively.@*CONCLUSION@#The c.2720delT(p.Leu907Argfs*39) and c.1387_1390del GTGC(p.Val463Profs*34) variants of FLNA gene may be the genetic cause of the three patients.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Convulsões / Imageamento por Ressonância Magnética / Epilepsia / Heterotopia Nodular Periventricular / Filaminas / Heterozigoto / Mutação Tipo de estudo: Guia de Prática Clínica Limite: Feminino / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2021 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Convulsões / Imageamento por Ressonância Magnética / Epilepsia / Heterotopia Nodular Periventricular / Filaminas / Heterozigoto / Mutação Tipo de estudo: Guia de Prática Clínica Limite: Feminino / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2021 Tipo de documento: Artigo