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Results 1 - 10 of 14 for Infantile spasms
  1. Developmental and epileptic encephalopathy 1 
    ... characterized by a type of seizure known as infantile spasms. The spasms usually appear before the age of ... sleeping, the spasms commonly occur just after awakening. Infantile spasms usually stop by age 5, but many children ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  2. 15q11-q13 duplication syndrome 
    ... affected individuals, seizures begin with a type called infantile spasms (seizures that usually appear before the age of ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  3. CDKL5 deficiency disorder 
    CDKL5 deficiency disorder is characterized by seizures that begin in infancy, followed by significant delays in many aspects of development.Seizures in CDKL5 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  4. Lennox-Gastaut syndrome 
    ... have a history of epilepsy beginning in infancy (infantile spasms) or a related condition called West syndrome before ... death among children with Lennox-Gastaut syndrome and infantile spasms. J Child Neurol. 2010 Apr;25(4):441- ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  5. Isolated lissencephaly sequence 
    ... with ILS have a type of seizure called infantile spasms, these seizures can be severe enough to cause ... develop a variety of seizure types, including persisting infantile spasms, short periods of loss of consciousness (absence seizures); ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  6. Aicardi syndrome 
    ... corpus callosum). They have seizures beginning in infancy (infantile spasms), which tend to progress to recurrent seizures (epilepsy) ... with chorioretinal abnormality Agenesis of corpus callosum with infantile spasms and ocular abnormalities Aicardi's syndrome Callosal agenesis ...
    https://medlineplus.gov/genetics/condition/aicardi-syndrome - Genetics
  7. Phosphoglycerate dehydrogenase deficiency 
    ... can vary in type. Recurrent muscle contractions called infantile spasms are typical early in the disorder. Without early treatment, seizures may progress to tonic-clonic seizures, which involve a loss of ... form of phosphoglycerate dehydrogenase deficiency develop many of ...
    https://medlineplus.gov/...phosphoglycerate-dehydrogenase-deficiency - Genetics
  8. CUL3-related neurodevelopmental disorder 
    ... associated with global developmental delays with or without infantile spasms. J Hum Genet. 2020 Sep;65(9):727- ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  9. SCN8A-related epilepsy with encephalopathy 
    ... involuntary muscle contractions that occur before age 1 (infantile spasms), partial or complete loss of consciousness (absence seizures), ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  10. SLC35A2-congenital disorder of glycosylation 
    ... months of life, usually involving uncontrollable muscle stiffening (infantile spasms) that can switch to shorter episodes of muscle ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
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