Congenital radioulnar synostosis
MONDO:0017985Congenital 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.
Also known as: radioulnar fusion, radioulnar synostosis, radioulnar synostosis (disease), 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
36 clinical trials for this condition and its sub-types.
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Broader categories
Disease
(618)
Musculoskeletal system disorder
(196)
Bone disorder
(47)
Human disease
(14)
Skeletal system disorder
(4)
Bone development disease
(2)
Synostosis
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disorder of development or morphogenesis
(0)