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Results 1 - 10 of 142 for Seizure Disorders
  1. SCN1A gene 
    ... seizures plus (GEFS+), which is a spectrum of seizure disorders of varying severity. These conditions include simple febrile ( ... or why they lead to a range of seizure disorders with varying severity. More About This Health Condition ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  2. DEPDC5 gene 
    ... Mutations in the DEPDC5 gene can cause other seizure disorders, known as familial mesial temporal lobe epilepsy and ... with mutations in the same gene develop different seizure disorders. DEP.5 FFEVF FFEVF1 KIAA0645 Tests of DEPDC5 ...
    https://medlineplus.gov/genetics/gene/depdc5 - Genetics
  3. GRIN2A gene 
    ... patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region. Epilepsia. 2010 Sep;51( ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  4. EPM2A gene 
    ... been identified in people with Lafora progressive myoclonus epilepsy. Many of these mutations change single protein building ... to the major features of Lafora progressive myoclonus epilepsy. Studies suggest that a loss of laforin prevents ...
    https://medlineplus.gov/genetics/gene/epm2a - Genetics
  5. CLN8 gene 
    ... of CLN8 disease is characterized by recurrent seizures (epilepsy) and a decline in intellectual function that begins ... a gradual worsening of motor and cognitive skills, epilepsy, and vision loss. In this form, signs and ...
    https://medlineplus.gov/genetics/gene/cln8 - Genetics
  6. SCN9A gene 
    ... gene called SCN1A, alter the progression of a seizure disorder called Dravet syndrome in some individuals. Dravet syndrome ... ALPHA SUBUNIT 9; SCN9A DRAVET SYNDROME; DRVT GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7 NCBI ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  7. TBC1D24 gene 
    ... have also been 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. CYP2C19 gene 
    ... to treat psychiatric disorders; anticonvulsants, used to treat seizure disorders; hypnotics and sedatives, used as sleep aids; antimalarial ...
    https://medlineplus.gov/genetics/gene/cyp2c19 - Genetics
  9. LETM1 gene 
    ... chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder. Epilepsia. 2014 Jun;55(6):849-57. doi: ...
    https://medlineplus.gov/genetics/gene/letm1 - Genetics
  10. CHRNB2 gene 
    ... in people with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE). Each of these mutations changes a single ... OK. The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. Neurobiol Dis. 2005 Dec; ...
    https://medlineplus.gov/genetics/gene/chrnb2 - Genetics
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