Results 1 -
10
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63
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Infantile epilepsy
- ... show signs and symptoms of the condition. Amish infantile epilepsy syndrome Epilepsy syndrome, infantile-onset symptomatic Ganglioside GM3 synthase deficiency Infantile-onset symptomatic epilepsy syndrome Genetic Testing Registry: GM3 synthase deficiency GM3 ...
- ... implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. Am J Med Genet ...
- ... implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. Am J Med Genet ...
- Tuberous Sclerosis Complex (For Parents) (Nemours Foundation)Tuberous Sclerosis/Children ... Tuberous Sclerosis ... Nemours Foundation ... tuberous sclerosis, tuberous sclerosis complex, TSC, hamartomas, tumors, neurology, ... Tuberous ...
- ... in 1892 to genetic linkage with benign familial infantile convulsions. Epilepsy Res. 2006 Aug;70 Suppl 1:S174-84. ...
- ... in people with other seizure disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations ...
- Seizures (Nemours Foundation)seizures, seizure, my child is having a seizure, my child had a seizure, sezure, siezure, seisure, siesure, consciousness, altered consciousness, loss ...
- First Aid: Seizures (Nemours Foundation)Seizures/Children ... Seizures ... Nemours Foundation ... seizures, seizure, seizure first aid, what to do if your child has a seizure, what if my child has a seizure, ...
- ... seizure disorders, known as familial mesial temporal lobe epilepsy and infantile spasms. Similar to individuals with FFEVF (described above), ... gene mutations that cause familial mesial temporal lobe epilepsy or infantile spasms lead to reduced GATOR1 complex formation and ...
- ... Dwek RA, Butters TD, Platt FM, Crosby AH. Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function ...