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Results 61 - 70 of 70 for Childhood epilepsy
  1. SLC35A2-congenital disorder of glycosylation 
    ... mutation in SLC35A2: Clinical features and treatment for epilepsy. Brain Dev. 2017 Mar;39(3):256-260. ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  2. Cerebrotendinous xanthomatosis 
    ... the brain. These neurological problems include recurrent seizures (epilepsy), movement disorders, impaired speech (dysarthria), loss of sensation ... of the eyes (cataracts) and chronic diarrhea in childhood; a reduced ability to produce and release a ...
    https://medlineplus.gov/.../condition/cerebrotendinous-xanthomatosis - Genetics
  3. Darier disease 
    ... have neurological disorders such as mild intellectual disabilities, epilepsy, and depression. Learning and behavior difficulties have also ...
    https://medlineplus.gov/genetics/condition/darier-disease - Genetics
  4. PPP2R5D-related intellectual disability 
    ... and walking; and delayed speech development. Recurrent seizures (epilepsy) and autism spectrum disorder, which is characterized by ... A, Elliott A, Ruark E, van Montfort R; Childhood Overgrowth Collaboration; Rahman N. Mutations in the PP2A ...
    https://medlineplus.gov/.../ppp2r5d-related-intellectual-disability - Genetics
  5. GABA-transaminase deficiency 
    ... infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled limb movements (choreoathetosis), exaggerated reflexes (hyperreflexia), weak ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  6. Dentatorubral-pallidoluysian atrophy 
    ... mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing ... Goto Y. Importance of CAG repeat length in childhood-onset dentatorubral-pallidoluysian atrophy. J Neurol. 2012 Nov; ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  7. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... the condition. Some affected individuals develop recurrent seizures (epilepsy), speech difficulties (dysarthria), learning problems, or mild deterioration ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  8. Farber lipogranulomatosis 
    ... disease and spinal muscular atrophy with progressive myoclonic epilepsy. Hum Mutat. 2020 Sep;41(9):1469-1487. ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  9. Dupuytren contracture 
    ... certain medications, such as those used to treat epilepsy (anticonvulsants); and previous injury to the hand. SFRP4 ...
    https://medlineplus.gov/genetics/condition/dupuytren-contracture - Genetics
  10. SETBP1 haploinsufficiency disorder 
    ... as sitting, standing, and walking; or recurrent seizures (epilepsy).Distinctive facial features in people with SETBP1 haploinsufficiency ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
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