Myoclonic epilepsy
An autosomal dominant condition caused by mutation(s) in the SLC6A1 gene, encoding sodium- and chloride-dependent GABA transporter 1. It is characterized by early onset of absence and myoclonic seizures following developmental delay. Intellectual disability may develop following the onset of seizures.
Disease Alternative Name
Recent Cases of Myoclonic epilepsy
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Top Myoclonic epilepsy Doctors on Curofy
Top doctors who continously share their opinions on Myoclonic epilepsy
Kerala Institute of Medical Sciences
Professor and Senior Consultant Neurology
Medical College Thiruvananthapuram
MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
Shadan Institute of Medical Sciences
Professor of Pediatric and Pediatric Neurologist
Medical College Trivandrum
fellowship in pediatric Neurology
LLRM
Senior Resident
Dhanvantri Children Hospital
Consultant
Mrmc
MBBS,,,DCH
59 Views
, 6 Answers