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Results 1 - 4 of 4 for "Epilepsy," familial adult "myoclonic," 3
Did you mean "Epilepsy," familial adult "mayoclinic," 3?
  1. 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. ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  2. Dentatorubral-pallidoluysian atrophy 
    ... s mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy ... Pericak-Vance MA, Vance JM. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521-4. ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  3. MT-TH gene 
    ... also have features of another mitochondrial disorder called myoclonic epilepsy with ragged-red fibers (MERRF); these additional features ... the MT-TH gene have features of both myoclonic epilepsy with ragged-red fibers (MERRF) and MELAS. The ...
    https://medlineplus.gov/genetics/gene/mt-th - 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