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Results 1 - 8 of 8 for Bilateral "tonic-clonic" seizure
  1. Polymicrogyria 
    ... paralysis. The most severe form of the disorder, bilateral generalized polymicrogyria, affects the entire brain. This condition causes severe intellectual disability, problems with movement, and seizures that are difficult or impossible to control with ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  2. ADGRG1 gene 
    ... people with a severe form of polymicrogyria called bilateral frontoparietal polymicrogyria (BFPP). This disorder causes intellectual disability, delayed development, problems with speech and movement, and recurrent seizures (epilepsy). Most of the identified mutations change a ...
    https://medlineplus.gov/genetics/gene/adgrg1 - Genetics
  3. Primary familial brain calcification 
    ... not show signs and symptoms of the condition. Bilateral striopallidodentate calcinosis Cerebrovascular ferrocalcinosis Familial idiopathic basal ganglia ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics
  4. Hartsfield syndrome 
    ... and split hand/foot syndrome Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Holoprosencephaly, hypertelorism, and ectrodactyly syndrome ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  5. RNAse T2-deficient leukoencephalopathy 
    ... condition. Cystic leukoencephalopathy without megalencephaly LBATC Leukoencephalopathy with bilateral anterior temporal lobe cysts RNASET2-deficient cystic leukoencephalopathy ...
    https://medlineplus.gov/.../rnase-t2-deficient-leukoencephalopathy - Genetics
  6. Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 
    ... is also associated with a brain abnormality called bilateral perisylvian polymicrogyria (BPP). The surface of the brain ... severe. About half of affected individuals develop recurrent seizures (epilepsy) beginning early in childhood. People with MPPH ...
    https://medlineplus.gov/...ogyria-polydactyly-hydrocephalus-syndrome - Genetics
  7. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... O. Rere controls retinoic acid signalling and somite bilateral symmetry. Nature. 2010 Feb 18;463(7283):953- ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  8. Coats plus syndrome 
    ... JB. Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- ...
    https://medlineplus.gov/genetics/condition/coats-plus-syndrome - Genetics