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SAS Journal of Surgery | Volume-10 | Issue-05
Congenital Radioulnar Synostosis, a Report of 7 Cases and Review of Literature
El Alouani El Mehdi, El Bardi Touria, El Alami El Fellous Sidi Zouhair
Published: May 31, 2024 | 39 37
DOI: 10.36347/sasjs.2024.v10i05.025
Pages: 635-641
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Abstract
Background: Congenital radio-ulnar synostosis is rare condition, characterized by limited pronation and supination. It is typically diagnosed in school-aged children. The forearm is mostly fixed in a hyperpronated position. Transverse derotational osteotomy at the site of synostosis is the intervention we propose. Patients and methods: This is a retrospective study including 7 cases of congenital radio-ulnar synostosis followed and treated at the pediatric orthopedic department of the children's Hospital of Rabat between January 2006 to February 2017. Results: The average age is about 32.5 months with a male predominance. Bilateral involvement presents 57.7% of cases. According to the Cleary and Omer classification, 42.8% of cases are classified as type IV, and 57.1% of cases are classified as type III. The average degree of preoperative fixed rotation of the forearm is 66° (from 0° to 85°). Only one patient presents a poly-malformative syndrome. Ten forearms underwent surgery, with transverse derotational osteotomy at the site of synostosis, without any postoperative complications.