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Advance in molecular genetic research on generalized epilepsies / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 908-911, 2018.
Artículo en Chino | WPRIM | ID: wpr-775806
ABSTRACT
Genetic generalized epilepsies (GGEs) are a group of epilepsy syndromes caused by genetic factors. A few of GGEs conform to the Mendelian patterns, while most of them show polygene inheritance. Researchers initially found that most of the genes associated with GGEs are related to ion channels including voltage-gated sodium channels, potassium channels, calcium channels and chloride channels, and ligand-gated gamma-aminobutyric acid receptor channels. Further researches have shown that certain non-ion channel genes are also related to GGEs, and that de novo mutations and copy number variants also play an important role in the pathogenesis of GGEs. Application of next- and third-generation sequencing promoted delineation of the molecular genetics of the GGEs, but also brought more challenges. Genetic findings have provided an important basis for the elucidation of the pathogenesis, clinical diagnosis and precise treatment of GGEs. This paper provided a review for recent progress made in molecular genetics of GGEs.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Epilepsia Generalizada / Investigación Genética / Genética / Canales Iónicos Límite: Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Epilepsia Generalizada / Investigación Genética / Genética / Canales Iónicos Límite: Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2018 Tipo del documento: Artículo