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Congenital radioulnar synostosis

ORPHA3269
Synonym(s) Radioulnar fusion
Prevalence Unknown
Inheritance Unknown
Age of onset Infancy
Childhood
ICD-10
  • Q74.0
OMIM
UMLS
  • C0431795
MeSH -
MedDRA -

Summary

Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and is characterized by failure of segmentation of the radius and ulna embryologically, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living.


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