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Results 31 - 40 of 63 for Infantile epilepsy
  1. Spinal muscular atrophy 
    ... 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
  2. CLN8 disease 
    CLN8 disease is an inherited disorder that varies in severity and primarily affects the nervous system. The condition is generally separated into less-severe ...
    https://medlineplus.gov/genetics/condition/cln8-disease - Genetics
  3. Developmental and epileptic encephalopathy 1 
    ... Frost JD Jr. Infantile epileptic encephalopathy with hypsarrhythmia (infantile ... based on molecular and cell biology. Epilepsy Res. 2006 Aug;70 Suppl 1:S87-95. ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  4. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy is a chronic brain disorder in which groups of nerve cells, or neurons, in the brain sometimes send the wrong signals and cause seizures. Epilepsy ( ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
  5. 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
  6. Isolated lissencephaly sequence 
    ... than 90 percent of individuals with ILS develop epilepsy, often within the first year of life. Up to 80 percent of infants with ILS have a type of seizure called infantile spasms, these seizures can be severe enough to ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  7. Infantile-onset spinocerebellar ataxia 
    Infantile-onset spinocerebellar ataxia (IOSCA) is a progressive disorder that affects the nervous system. Babies with IOSCA ... hypotonia, ataxia, hypacusis, and athetosis Genetic Testing Registry: Infantile onset spinocerebellar ataxia Infantile-onset spinocerebellar ataxia Mitochondrial ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  8. Myoclonic epilepsy with ragged-red fibers 
    ... tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. Neurogenetics. 2012 Aug;13(3): ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  9. SCN8A gene 
    ... can cause movement problems and seizures called benign infantile seizures, which ... BFIS5 CERIII CIAT hNa6/Scn8a voltage- ...
    https://medlineplus.gov/genetics/gene/scn8a - Genetics
  10. CLN2 disease 
    ... symptoms of the condition. Jansky-Bielschowsky disease Late-infantile Batten disease Late-infantile neuronal ceroid lipofuscinosis LINCL Neuronal ceroid lipofuscinosis, late- ...
    https://medlineplus.gov/genetics/condition/cln2-disease - Genetics
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