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Results 11 - 20 of 63 for Infantile epilepsy
  1. KCNB1 encephalopathy 
    ... 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
  2. Seizures (National Library of Medicine)  
    Seizures are symptoms of a brain problem. They happen because of sudden, abnormal electrical activity in the brain. When people think of seizures, they often ...
    https://medlineplus.gov/seizures.html - Health Topics
  3. Epilepsy (National Library of Medicine)  
    Epilepsy is a brain disorder that causes people to have recurring seizures. The seizures happen when clusters of nerve cells, or neurons, in the brain send out ...
    https://medlineplus.gov/epilepsy.html - Health Topics
  4. SCN8A-related epilepsy with encephalopathy 
    ... begin in infancy.The seizures in SCN8A-related epilepsy with encephalopathy include involuntary muscle contractions that occur before age 1 (infantile spasms), partial or complete loss of consciousness (absence ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  5. Central Nervous System: The Brain and Spinal Cord (Nemours Foundation)  
    ... movements, speech, balance, coordinations, bell's palsy, brain tumors, epilepsy, infantile spasms, holoprosencephaly, seizures, mental illnesses, depressions, headaches, migraines, ...
    https://kidshealth.org/en/parents/central-nervous-system.html - External Health Links
  6. CACNA1A gene 
    ... 13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms. Epilepsia. 2009 Nov;50(11):2501-3. ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  7. 19p13.13 deletion syndrome 
    ... 13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms. Epilepsia. 2009 Nov;50(11):2501-3. ...
    https://medlineplus.gov/genetics/condition/19p1313-deletion-syndrome - Genetics
  8. Malignant migrating partial seizures of infancy 
    ... embryonic development (called a de novo mutation). Early infantile epileptic encephalopathy 14 EIEE14 Malignant migrating partial epilepsy of infancy Migrating partial epilepsy of infancy Migrating ...
    https://medlineplus.gov/...ant-migrating-partial-seizures-of-infancy - Genetics
  9. STXBP1 encephalopathy 
    ... 4 Developmental and epileptic encephalopathy, type 4 Early-infantile epileptic encephalopathy 4 EIEE4 STXBP1 encephalopathy with epilepsy STXBP1 epileptic encephalopathy STXBP1-related developmental and epileptic ...
    https://medlineplus.gov/genetics/condition/stxbp1-encephalopathy - Genetics
  10. Birth Disorders of the Brain and Spinal Cord From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Neural Tube Defects/Specifics ... Neural Tube Defects ... Brain Diseases/Specifics ... Brain Diseases ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Craniofacial ...
    https://www.ninds.nih.gov/.../birth-disorders-brain-and-spinal-cord - External Health Links
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