Osteogenesis imperfecta type 1 with an incidental finding of bilateral radioulnar synostosis-Reference-Cited by-同舟云学术

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Osteogenesis imperfecta type 1 with an incidental finding of bilateral radioulnar synostosis

Published:2020-04-08 Issue:3 Volume:29 Page:155-157
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Apperley Louise J.,Richmond Stacey,Ramakrishnan Renuka,Balasubramanian Meena

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Congenital radioulnar synostosis. Radiological characteristics and hand function: case reports.;Bauer;Scand J Plast Reconstr Surg Hand Surg,1988

2. Pathophysiology and therapeutic options in osteogenesis imperfecta: an update.;Brizola;Research and Reports in Endocrine Disorders,2016

3. Congenital proximal radioulnar synstosis.;Dogra;IJPS,2003

4. Surgical treatment of congenital radioulnar synostosis in children: a case report.;El Bakkaly;International Journal of Surgery and Medicine,2018

5. Derotation osteotomy for congenital radioulnar synostosis.;ElSayed;Orthopaedic J,2014

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