Three Indian siblings affected with progressive myoclonic epilepsy due to unverricht–Lundborg disease

Background: Progressive myoclonus epilepsy (PME) is a group of heterogeneous genetic disorders characterized by action myoclonus, epileptic seizures, and progressive neurologic deterioration with onset of symptoms in adolescence and adulthood. Unverricht–Lundborg disease (ULD) is the most common typ...

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Autori principali:	Kavita Srivastava, Bina Mahendrasinh Thakor, Shuvendu Roy, Surekha Rajadhyaksha, Chaitanya Datar
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Wolters Kluwer Medknow Publications 2022-01-01
Serie:	Indian Pediatrics Case Reports
Soggetti:	action myoclonus generalized epilepsy progressive myoclonic epilepsy unverricht–lundborg disease
Accesso online:	http://www.ipcares.org/article.asp?issn=2772-5170;year=2022;volume=2;issue=1;spage=7;epage=11;aulast=Srivastava
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