(?) CONGENITAL SYNOSTOSIS.

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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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Congenital distal tibiofibular synostosis

Congenital distal tibiofibular synostosis is a very rare anomaly. The cases of congenital tibiofibular synostosis reported in the literature so far have been confined to the proximal tibiofibular joint. We present an unusual case of tibiofibular synostosis that involves the distal part of the tibia and fibula based on characteristic X-ray, CT, and MRI findings.

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Congenital radioulnar synostosis – case report

BACKGROUND Congenital radioulnar synostosis is a rare malformation of the upper limb, with functional limitations of the limb. CASE REPORT A 10-year-old child with pain and restricted mobility of the elbow joint was admitted to the hospital. Plain film radiography and CT examination was performed. Radiological examinations showed a congenital radioulnar synostosis. The child underwent surgica...

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Radiographic assessment of congenital C2-3 synostosis.

PURPOSE To evaluate the morphologies of congenital C2-3 synostosis in 25 patients. METHODS Radiographs of 11 males and 14 females aged 5 to 74 years with congenital C2-3 synostosis were reviewed. All cases were found incidentally on radiographs when presenting with neck/shoulder discomfort/pain. RESULTS 13 of the patients had spondylosis in 21 segments: C1-2 (n=1) and C3-4 (n=1), C4-5 (n=7)...

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Rotational osteotomies for congenital radioulnar synostosis.

In five children, six forearms with a fixed pronation deformity secondary to congenital radioulnar synostosis were treated by a derotation osteotomy of the distal radius and the midshaft of the ulna. There were three boys and two girls with a mean age of 4.9 years (3.5 to 8.25) who were followed up for a mean of 29 months (18 to 43). The position of the forearm was improved from a mean pronatio...

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ژورنال

عنوان ژورنال: The Lancet

سال: 1919

ISSN: 0140-6736

DOI: 10.1016/s0140-6736(00)45945-3