Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 12 for Familial infantile myoclonic epilepsy
Did you mean Familial infantile mayoclinic epilepsy?
  1. TBC1D24 gene 
    ... identified in people with other seizure disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  2. ARX gene 
    ... JL. ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. Am J Med Genet ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  3. Myoclonic epilepsy with ragged-red fibers 
    ... mitochondrial gene and occurs in people with no family history of MERRF. Fukuhara disease MERRF MERRF syndrome Myoclonic epilepsy associated with ragged-red fibers Myoencephalopathy ragged-red ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  4. Spinal muscular atrophy 
    ... diseases, such as spinal muscular atrophy with progressive myoclonic epilepsy, spinal muscular atrophy with lower extremity predominance, X-linked infantile spinal muscular atrophy, and spinal muscular atrophy with ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  5. KCNB1 encephalopathy 
    ... with no history of the disorder in their family. Early infantile epileptic encephalopathy 26 EIEE26 Epileptic encephalopathy, early infantile, 26 KCNB1-related epilepsy Genetic Testing Registry: Developmental and epileptic encephalopathy, 26 ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  6. Spinal Muscular Atrophy (National Library of Medicine)  
    What is spinal muscular atrophy (SMA)? Spinal muscular atrophy (SMA) is a group of genetic diseases that damages and kills motor neurons. Motor neurons ...
    https://medlineplus.gov/spinalmuscularatrophy.html - Health Topics
  7. SCN8A-related epilepsy with encephalopathy 
    ... begin in infancy.The seizures in SCN8A-related epilepsy with encephalopathy ... (myoclonic seizures), or loss of consciousness with muscle rigidity ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  8. STXBP1 encephalopathy 
    ... with no history of the disorder in their family. ... with epilepsy STXBP1 epileptic encephalopathy STXBP1-related developmental and epileptic ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  9. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Start Here ... Epilepsy ... Seizures/Start Here ... Seizures ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Epilepsy ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
  10. 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 - External Health Links
previous · 1 · 2 · next