| syndroom van hemidystonie en hemiatrofie (aandoening) | | syndroom van hemidystonie en hemiatrofie | | Hemidystonia hemiatrophy syndrome | | A rare dystonia with a combination of hemidystonia involving one half of the body and hemiatrophy on the same side. Hemidystonia which is sustained and repetitive muscle contractions resulting in abnormal movements or posture involving a single side of the body is preceded in 90% of cases by hemiparesis with a marked improvement before the onset of hemidystonia. Pyramidal syndrome and seizures may also be observed. The syndrome is associated with ipsilateral somatic atrophy. Common causes are childbirth or perinatal complications, delayed sequelae of stroke or head trauma. This syndrome should be differentiated from other causes of primary dystonia or dystonia secondary to inherited disorders or neurodegenerative diseases. |
| | Id | 724383002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G24.8 | | Term | Overige gespecificeerde vormen van dystonie |
| Target | G23.8 | | Term | Overige gespecificeerde degeneratieve ziekten van basale ganglia |
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| SNOMED CT to Orphanet simple map | 306741 |
| SNOMED CT to ICD-10 extended map | | Target | G24.8 | | Rule | TRUE | | Advice | ALWAYS G24.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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