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Results 1 - 6 of 6 for Juvenile myoclonic epilepsy
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  1. Juvenile myoclonic epilepsy 
    Juvenile myoclonic epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood or adolescence, usually ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  2. EFHC1 gene 
    ... identified in a small number of people with juvenile myoclonic epilepsy. This condition typically begins in childhood or adolescence ... and absence seizures. Most gene mutations associated with juvenile myoclonic epilepsy replace single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/efhc1 - Genetics
  3. GABRA1 gene 
    ... been identified in at least one family with juvenile myoclonic epilepsy. This condition typically begins in childhood or adolescence ... of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy. Nat Genet. 2002 Jun;31(2):184-9. ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  4. CLCN2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Juvenile myoclonic epilepsy More About This Health Condition chloride channel 2 ...
    https://medlineplus.gov/genetics/gene/clcn2 - Genetics
  5. Phosphoglycerate dehydrogenase deficiency 
    ... a loss of consciousness, muscle rigidity, and convulsions; myoclonic seizures, ... have epilepsy as well as mild developmental delay and intellectual ...
    https://medlineplus.gov/...phosphoglycerate-dehydrogenase-deficiency - Genetics
  6. CLN5 disease 
    ... include recurrent seizures that involve uncontrollable muscle jerks (myoclonic epilepsy), difficulty coordinating movements (ataxia), vision loss, speech problems, ...
    https://medlineplus.gov/genetics/condition/cln5-disease - Genetics