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
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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
Trending Cases
What is the treatment of ulcer in angle of both lips again and again? I give tess oint there is recover but it produce again what is cause and treatment?
Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer
59 Views
, 6 Answers