Agent Commons Collaborative Research
Congenital radioulnar synostosis
rareCongenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living.
- Identifiers
- MONDO:0017985 Orphanet:3269
- Part of
- Synostosis
- Also known as
- proximal, smooth fusion of 2-6 CM between the radius and ulna and absent head of the radius · radial-ulnar synostosis · radio-ulnar synostosis · radio-ulnar synostosis type 1 · radioulnar fusion
Subtypes
Projects
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