| syndroom van infantiele convulsie en choreoathetose (aandoening) | | syndroom van infantiele convulsie en choreoathetose | | syndroom van infantiel insult en choreoathetose
ICCA-syndroom
syndroom van infantiele epileptische aanval en choreoathetose
paroxismale kinesiogene dyskinesie en infantiele convulsie
| | ICCA syndrome | | Infantile convulsion and choreoathetosis syndrome
Paroxysmal kinesigenic dyskinesia and infantile convulsion
| | A rare neurological condition with manifestation of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence. Benign familial infantile epilepsy begins at 3 to 12 months of age with a family history of the same type of seizures. Seizures are afebrile and normally disappear after the first year of life. During childhood or adolescence, affected individuals present with paroxysmal kinesigenic dyskinesia with frequent and recurrent episodic choreathetotic or dystonic movements that last less than 1 minute. Can present as sporadic or familial, in the latter case, it is transmitted as an autosomal dominant trait that can be variably expressed within the same family. |
| | Id | 715534008 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G40.4 | | Term | Overige vormen van gegeneraliseerde epilepsie en epileptische syndromen |
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| SNOMED CT to Orphanet simple map | 31709 |
| SNOMED CT to ICD-10 extended map | | Target | G40.4 | | Rule | TRUE | | Advice | ALWAYS G40.4 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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