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Results 1 - 10 of 26 for Early onset absence seizures
  1. LAMA2-related muscular dystrophy 
    ... Most LAMA2 gene mutations that cause the severe, early-onset form of LAMA2-related muscular dystrophy result in the absence of functional laminin alpha-2 subunit. Mutations that ...
    https://medlineplus.gov/.../lama2-related-muscular-dystrophy - Genetics
  2. Aicardi-Goutieres Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Aicardi-Goutières ...
    https://www.ninds.nih.gov/.../disorders/aicardi-goutieres-syndrome - External Health Links
  3. Lennox-Gastaut Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Epilepsy/Specifics ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Lennox-Gastaut syndrome is a severe ...
    https://www.ninds.nih.gov/.../disorders/lennox-gastaut-syndrome - External Health Links
  4. Travelers' Health: Extremes of Temperature (Centers for Disease Control and Prevention)  
    Traveler's Health/Related Issues ... Traveler's Health ... Centers for Disease Control and Prevention ... Information about how to order the U.S. government publication ...
    https://wwwnc.cdc.gov/.../extremes-of-temperature - External Health Links
  5. Epilepsy-aphasia spectrum 
    ... half of children with ECSWS develop normally in early childhood, while others have ... absence seizures, which involve short periods of staring blankly; ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  6. STXBP1 encephalopathy 
    ... STXBP1-related developmental and epileptic encephalopathy STXBP1-related early-onset encephalopathy STXBP1-related epileptic encephalopathy Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  7. 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 ... Request free mailed brochure ... From the National Institutes ...
    https://www.ninds.nih.gov/.../curing-epilepsies-promise-research - External Health Links
  8. Beta-propeller protein-associated neurodegeneration 
    ... who have been diagnosed with intellectual disability or early-onset parkinsonism based on their signs and symptoms have ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  9. CHD2 myoclonic encephalopathy 
    ... atonic seizures); partial or complete loss of consciousness (absence seizures); seizures brought on by high body temperature (febrile ... experience a type of seizure called atonic-myoclonic-absence seizure, which begins with a drop of the head, ...
    https://medlineplus.gov/.../condition/chd2-myoclonic-encephalopathy - Genetics
  10. Epilepsy and Seizures From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Seizures/Start Here ... Seizures ... Epilepsy/Start Here ... Epilepsy ... Epilepsy is a chronic brain disorder in which groups of nerve cells, or neurons, in the brain sometimes ...
    https://www.ninds.nih.gov/.../disorders/epilepsy-and-seizures - External Health Links
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