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Results 1 - 10 of 10 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. Levetiracetam 
    ... combination with other medications to treat seizure in adults and children 12 years of age or older with juvenile myoclonic epilepsy. Levetiracetam is also used in combination with other ...
    https://medlineplus.gov/druginfo/meds/a699059.html - Drugs and Supplements
  3. Levetiracetam Injection 
    ... combination with other medications to treat seizures in adults and children 12 years of age or older with juvenile myoclonic epilepsy who cannot take oral medications. Levetiracetam injection is ...
    https://medlineplus.gov/druginfo/meds/a622013.html - Drugs and Supplements
  4. 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
  5. Curing the Epilepsies: The Promise of Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Statistics and Research ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Curing the Epilepsies: ...
    https://www.ninds.nih.gov/.../curing-epilepsies-promise-research - National Institutes of Health
  6. 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
  7. 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
  8. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Seizures/Start Here ... Seizures ... Epilepsy/Start Here ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Epilepsy ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - National Institutes of Health
  9. Landau-Kleffner Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Aphasia/Children ... Aphasia ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about Landau- ...
    https://rarediseases.info.nih.gov/.../6855/landau-kleffner-syndrome - National Institutes of Health
  10. Absence Seizure (Petit Mal Seizure) (Mayo Foundation for Medical Education and Research)  
    Seizures/Specifics ... Seizures ... Mayo Foundation for Medical Education and Research
    https://www.mayoclinic.org/.../symptoms-causes/syc-20359683?p=1 - External Health Links