Isolated congenital radial head dislocation
Synonyms: Isolated congenital elbow dislocation
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital limb malformation characterized by mostly posterior, less frequently also anterior or lateral dislocation of the radial head from its position in the humeroradial joint. It is bilateral in the majority of cases and can occur as an isolated feature or in association with other congenital malformations and as part of a number of syndromes. The defect may at first cause only mild symptoms such as pain and limitation of flexion of the elbow, but may eventually lead to joint instability, dysplastic changes of the radial head, and arthritis.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated congenital radial head dislocation | Isolated congenital elbow dislocation |
| fr | Luxation congénitale isolée de la tête radiale | Luxation congénitale isolée du coude |
| de | Radiuskopfdislokation, kongenitale, isolierte | Ellenbogendislokation, kongenitale, isolierte · Radiuskopfdislokation, kongenitale |
| es | Luxación congénita aislada de la cabeza radial | Luxación congénita aislada del codo |
| it | Dislocazione congenita isolata della testa del radio | Dislocazione congenita della testa del radio |
| nl | Geïsoleerde congenitale luxatie van radiuskop | Geïsoleerde congenitale elleboogluxatie |
| pt | Luxação congénita do cotovelo | Luxação congénita da cabeça do rádio |
| pl | Wrodzone zwichnięcie stawu łokciowego | Wrodzone zwichnięcie głowy kości promieniowej |
| cs | Vrozená dislokace lokte | Vrozená dislokace hlavice radia |
| uk | Ізольований вроджений вивих головки променевої кістки | Ізольований вроджений вивих ліктьового суглоба |
| zh | 孤立性先天性桡骨头脱位 | 孤立性先天性肘关节脱位 |
| tr | İzole doğumsal radyal baş çıkığı | Doğumsal izole dirsek çıkığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q68.8 | NTBT | inclusion | validated |
| ICD-11 | LB92 | E | specific | validated |
| MONDO | 0017469 | E | validated | |
| MONDO | 17469 | E | validated | |
| UMLS | C0265563 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:294951Congenital joint dislocations
rare developmental anomalies during embryogenesis; rare genetic diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295032
- This record as JSON: /data/d/295032.json