| Symbol
| ICCA
|
| Location
| 16p11.2
|
| HGNC id
| 5349
|
| Name
|
convulsions, familial infantile with paroxysmal choreoathetosis |
| Other name(s)
|
epilepsy, benign, neonatal 4
ICCA syndrome |
| Corresponding gene
|
PRRT2
|
| Other symbol(s)
| EBN4, FICCA, BFIC2
|
| Main clinical features
|
clusters of a febrile seizures occurring around the sixth month of life, with a benign course, a normal development and rare seizures in adulthood
associated or not with variably expressed paroxysmal choreoathetosis |
| Genetic determination
| autosomal dominant |
| Function/system disorder
| neurology |
| Type
| disease
|