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Results 1 - 4 of 4 for "Epilepsy," familial adult "myoclonic," 4
Did you mean "Epilepsy," familial adult "mayoclinic," 4?
  1. GABRA1 gene 
    ... The primary role of GABA in children and adults is to prevent the brain from being overloaded ... myoclonic epilepsy. This condition typically begins in childhood or adolescence ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  2. Lennox-Gastaut syndrome 
    ... people worldwide. This condition accounts for 3 to 4 percent of cases of epilepsy in children and 1 to 2 percent of cases in adults. For unknown reasons, it appears to be more ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  3. CLN4 disease 
    ... with no history of the disorder in their family. Adult neuronal ceroid lipofuscinosis Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant CLN4B Parry disease Genetic Testing Registry: Ceroid lipofuscinosis, neuronal, 4 (Kufs type) Adult neuronal ceroid lipofuscinosis National Organization ...
    https://medlineplus.gov/genetics/condition/cln4-disease - Genetics
  4. Dentatorubral-pallidoluysian atrophy 
    ... mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy ... syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521-4. doi: 10.1038/ng0894-521. Citation ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics