Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 16 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. 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
  7. SCN8A-related epilepsy with encephalopathy 
    ... begin in infancy.The seizures in SCN8A-related epilepsy with encephalopathy include involuntary muscle contractions that occur before age 1 (infantile spasms), partial or complete loss of consciousness (absence seizures), involuntary ...
    https://medlineplus.gov/...cn8a-related-epilepsy-with-encephalopathy - Genetics
  8. KCNB1 encephalopathy 
    ... with no history of the disorder in their family. Early infantile epileptic encephalopathy 26 EIEE26 Epileptic encephalopathy, early infantile, 26 KCNB1-related epilepsy Genetic Testing Registry: Developmental and epileptic encephalopathy, 26 ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - 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 at night during sleep. They are described as partial seizures because they affect only one area of ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  10. 16p11.2 deletion syndrome 
    ... Some people with this disorder have recurrent seizures (epilepsy).Some affected individuals have minor physical abnormalities such as low-set ears or partially webbed toes (partial syndactyly). People with this disorder are also at ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
previous · 1 · 2 · next