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Results 1 - 10 of 10 for Intractable seizure
  1. Molybdenum cofactor deficiency 
    ... develop seizures that do not improve with treatment (intractable seizures). Brain abnormalities, including deterioration (atrophy) of brain tissue, ...
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency - Genetics
  2. Microcephaly-capillary malformation syndrome 
    ... CL. A new syndrome with multiple capillary malformations, intractable seizures, and brain and limb anomalies. Am J Med ...
    https://medlineplus.gov/...rocephaly-capillary-malformation-syndrome - Genetics
  3. 15q11-q13 duplication syndrome 
    ... Affected individuals may develop complex, difficult-to-treat (intractable) seizure patterns such as Lennox-Gastaut syndrome. Seizures can ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  4. Isolated sulfite oxidase deficiency 
    ... sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia. Brain Dev. 2010 Aug;32( ...
    https://medlineplus.gov/.../isolated-sulfite-oxidase-deficiency - Genetics
  5. PHGDH gene 
    ... head size (microcephaly), severe developmental delay, and recurrent seizures that are difficult to treat (intractable epilepsy). Most of the mutations that cause this ...
    https://medlineplus.gov/genetics/gene/phgdh - Genetics
  6. Alpers-Huttenlocher syndrome 
    ... this condition usually have three characteristic features: recurrent seizures that do not improve with treatment (intractable epilepsy), loss of mental and movement abilities (psychomotor ...
    https://medlineplus.gov/.../condition/alpers-huttenlocher-syndrome - Genetics
  7. MTOR gene 
    ... cause focal cortical dysplasia type II leading to intractable epilepsy. Nat Med. 2015 Apr;21(4):395- ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  8. Ring chromosome 20 syndrome 
    ... S, Ozkinay F. Ring chromosome 20 syndrome with intractable epilepsy. Dev Med Child Neurol. 2005 May;47( ... with severe phenotypic features followed for 25 years. Seizure. 2006 Sep;15(6):449-53. doi: 10. ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  9. ARX gene 
    ... abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". J ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  10. X-linked lissencephaly with abnormal genitalia 
    ... abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". J ...
    https://medlineplus.gov/...ked-lissencephaly-with-abnormal-genitalia - Genetics