Bilateral Congenital Radioulnar Synostosis - Case Report

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Authors: Derek DiAngelis, Matthew J Hudson
Cited by: 0

Abstract

A 2-year-old male presented to an orthopedic outpatient office due to a supination defect in both of his upper limbs. X-rays of the affected limbs revealed fusion of the proximal radioulnar joints indicating congenital radioulnar synostosis (CRUS). CRUS is abnormal development of the upper limbs occurring during weeks 3—7 of embryological development. Causes of CRUS include genetic syndromes and spontaneous mutations. Treatment options include nonoperative and surgical treatments, however, treatment is controversial due to a lack of clinical evidence. Proposed screening methods could help improve detection rates and improve clinical management. This report aims to increase awareness of CRUS and discuss evolving treatment options.

Fields of Study & Subjects

Congenital limb and hand anomalies Craniofacial Disorders and Treatments Elbow and Forearm Trauma Treatment

Publication details

Journal / source
Advances in Clinical Medical Research and Healthcare Delivery
Volume
6
Issue
1
Pages
37–40
Publication date
1 February 2026
Language
EN