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Results 1 - 10 of 23 for Familial partial epilepsy
  1. Familial focal epilepsy with variable foci 
    ... DEPDC5 gene mutations go on to develop FFEVF. Familial partial epilepsy with variable foci FFEVF Partial epilepsy with variable foci Genetic Testing Registry: Epilepsy, familial focal, with variable foci 1 Genetic Testing Registry: ...
    https://medlineplus.gov/...amilial-focal-epilepsy-with-variable-foci - Genetics
  2. Genetic epilepsy with febrile seizures plus 
    ... Li BM, Liao WP. Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures. Genes Brain Behav. 2012 ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  3. Autosomal dominant epilepsy with auditory features 
    ... Pedley TA, Hauser WA, Ottman R. Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to ...
    https://medlineplus.gov/...-dominant-epilepsy-with-auditory-features - Genetics
  4. Epilepsy-aphasia spectrum 
    ... with no history of the disorder in their family. Acquired aphasia with epilepsy DEE/EE-SWAS Developmental and/or epileptic encephalopathy ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  5. Epilepsy of infancy with migrating focal seizures 
    ... with migrating focal seizure in infancy Malignant migrating partial epilepsy of infancy Malignant migrating partial seizures of infancy MFSI Migrating focal seizures of infancy Migrating partial epilepsy of infancy Migrating partial seizures of infancy MMPEI ...
    https://medlineplus.gov/...-of-infancy-with-migrating-focal-seizures - Genetics
  6. LGI1 gene 
    ... Gilliam TC. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar;30( ... TA, Hauser WA. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13;62( ...
    https://medlineplus.gov/genetics/gene/lgi1 - Genetics
  7. TBC1D24 gene 
    ... identified in people with other seizure disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  8. Chromosome 20 
    ... on PubMed Oppenheimer S, Dignan P, Soukup S. Partial trisomy 20p: familial occurrence. Am J Med Genet. 2000 Dec 11; ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  9. ARX gene 
    ... JL. ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. Am J Med Genet ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  10. Lennox-Gastaut syndrome 
    ... percent of people with this condition have a family history of some type of epilepsy, indicating that inherited genetic factors may play a ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
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