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Results 1 - 10 of 90 for Childhood epilepsy
  1. Childhood absence epilepsy 
    Childhood absence epilepsy is a condition characterized by recurrent seizures (epilepsy). This condition begins in childhood, usually between ages 3 and 8. Affected ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics
  2. Epilepsy-aphasia spectrum 
    ... dyspraxia (ADRESD), intermediate epilepsy-aphasia disorder (IEAD), atypical childhood epilepsy with centrotemporal spikes (ACECTS), and childhood epilepsy with ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  3. GRIN2A gene 
    ... at the severe end of the spectrum, while childhood epilepsy with centrotemporal spikes (CECTS) is at the mild ... GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  4. GABRA1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Childhood absence epilepsy More About This Health Condition ECA4 EJM EJM5 ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  5. Polymicrogyria 
    ... Ohta H, Abiru K, Nakano K, Oka E. Childhood-onset epilepsy associated with polymicrogyria. Brain Dev. 2002 Dec;24( ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  6. GLUT1 deficiency syndrome 
    ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain. 2019 ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  7. CDKL5 deficiency disorder 
    ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain. 2019 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  8. CUL3-related neurodevelopmental disorder 
    ... or GERD), which tends to go away after childhood. Rarely, recurrent seizures (epilepsy), congenital heart abnormalities, or genitourinary abnormalities occur in ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  9. Ring chromosome 20 syndrome 
    ... common feature of this condition is recurrent seizures (epilepsy) in childhood. The seizures may occur during the day or ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  10. Koolen-de Vries syndrome 
    ... They usually have weak muscle tone (hypotonia) in childhood. About half have recurrent seizures (epilepsy).Affected individuals often have distinctive facial features including ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
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