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Results 1 - 5 of 5 for "Epilepsy," familial adult "myoclonic," 7
Did you mean "Epilepsy," familial adult "mayoclinic," 7?
  1. Dentatorubral-pallidoluysian atrophy 
    ... s mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy ... Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521-4. doi: 10.1038/ng0894-521. ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  2. 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
  3. Lennox-Gastaut syndrome 
    ... Undlien DE, Brodtkorb E. SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features. Epilepsy Behav. 2009 Nov;16(3):555-7. doi: 10.1016/j.yebeh.2009.08.021. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  4. CLN4 disease 
    ... disease often develop seizures and uncontrollable muscle jerks (myoclonic epilepsy), a decline in intellectual function (dementia), problems with ... with no history of the disorder in their family. Adult neuronal ceroid lipofuscinosis Ceroid lipofuscinosis, neuronal, 4B, autosomal ...
    https://medlineplus.gov/genetics/condition/cln4-disease - Genetics
  5. Dementia (National Library of Medicine)  
    What is dementia? Dementia is a loss of mental functions that is severe enough to affect your daily life and activities. These functions include: Memory ...
    https://medlineplus.gov/dementia.html - Health Topics