Familial radioulnar synostosis.
نویسنده
چکیده
A family with proximal radioulnar synostosis segregating in three generations is described. Familial radioulnar synostosis is a rare anomaly; however, the sporadic form is a frequent feature in cases of sex chromosome abnormalities and other syndromes. This disorder has been reported in several ethnic groups, but this is apparently the first example from the black population.
منابع مشابه
Congenital radioulnar synostosis
Congenital radioulnar synostosis is a rare disorder resulting in the fusion of the radius and ulna from birth. Management is conservative. Operative treatment rarely succeeds.
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Acute elbow extension deficit is an unusual phenomenon that has been observed in patients with congenital radioulnar synostosis. We report the case of an 11-year-old girl with congenital radioulnar synostosis who developed acute extension deficit of the right elbow and whose elbow range of motion was restored following lateral capsular release.
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عنوان ژورنال:
- Journal of medical genetics
دوره 15 2 شماره
صفحات -
تاریخ انتشار 1978