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Results 1 - 10 of 72 for Epilepsy with generalized "tonic-clonic" seizures
  1. SCN1A gene 
    ... SCN1A gene have been found to cause genetic epilepsy with febrile seizures plus (GEFS+), which is a spectrum of seizure ... VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 1; SCN1A GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2 GENERALIZED EPILEPSY WITH FEBRILE ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  2. PURA gene 
    ... weak muscle tone (hypotonia), breathing problems, recurrent seizures (epilepsy) or seizure-like episodes, and distinctive facial features. The deletion ...
    https://medlineplus.gov/genetics/gene/pura - Genetics
  3. SCN9A gene 
    ... Health Condition MedlinePlus Genetics provides information about Genetic epilepsy with febrile seizures plus More About This Health Condition MedlinePlus Genetics ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  4. CHD2 gene 
    ... CHD2 myoclonic encephalopathy, a condition characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability beginning ...
    https://medlineplus.gov/genetics/gene/chd2 - Genetics
  5. DEPDC5 gene 
    ... described above), people with familial mesial temporal lobe epilepsy have focal seizures. They may also have feelings of déjà vu, ... gene mutations that cause familial mesial temporal lobe epilepsy or infantile spasms lead to reduced GATOR1 complex formation ... Tests of ...
    https://medlineplus.gov/genetics/gene/depdc5 - Genetics
  6. GRIN2A gene 
    ... other developmental skills; and in many cases, recurrent seizures (epilepsy). Landau-Kleffner syndrome (LKS) and epileptic encephalopathy with ... language problems. These shared features can include recurrent seizures (epilepsy), often of a type that originates from abnormal ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  7. KCNQ2 gene 
    ... neonatal seizures (BFNS), a condition characterized by recurrent seizures (epilepsy) in newborn babies. The seizures begin around day 3 of life and usually ...
    https://medlineplus.gov/genetics/gene/kcnq2 - Genetics
  8. SCN8A gene 
    ... with encephalopathy. This condition is characterized by recurrent seizures (epilepsy), abnormal brain function (encephalopathy), and intellectual disability. The ...
    https://medlineplus.gov/genetics/gene/scn8a - Genetics
  9. POLG gene 
    ... sensory ataxia (MEMSA), which is characterized by recurrent seizures (epilepsy), muscle weakness (myopathy), and problems with coordination and ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
  10. NPRL2 gene 
    ... FFEVF), which is an uncommon form of recurrent seizures (epilepsy) that runs in families. Most of these mutations lead to the production of an abnormally short, nonfunctional protein. As a ... to the seizures of FFEVF. Research suggests that increased mTOR pathway ...
    https://medlineplus.gov/genetics/gene/nprl2 - Genetics
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