Article not rated

Vol. 9 - Num. 34

Clinical Reviews

Dysplasia capitis femoris (Meyer dysplasia)

V Toro Méndez, I O’Mullony Muñoz, JL Castilla Cubero, JA Conejero Casares

Reference of this article: Toro Méndez V, O’Mullony Muñoz I, Castilla Cubero JL, Conejero Casares JA. Dysplasia capitis femoris (Meyer dysplasia). Rev Pediatr Aten Primaria. 2007;9: 237-43.

Published in Internet: 30-06-2007 - Visits: 13221


Meyer?s dysplasia is an alteration in the development of infant hips, frequently misdiagnosed, characterized by irregularity and delay of ossification of the capital femoral epiphysis nucleus. Clinical observation: three case histories, which diagnostic criteria are compatible with Meyer?s syndrome, were located and initially diagnosed as Perthes disease or avascular necrosis of the femoral head. The patients were diagnosed because of pelvic oblicuity from birth. In their evolution, a delay was observed in ossification of the femoral head and a nucleus fragmentation at age 2. The patients remained asymptomatic throughout their follow up and remained under observation as the only treatment. Discussion: controversy exists in distinguishing diagnosis between Meyer?s syndrome and Perthes disease, where some authors point at different syndromes or different manifestations of the same illness. Its importance takes root in distinguishing diagnosis between Perthes disease and avascular necrosis after treating hip displasia to avoid unnecessary diagnostic tests and treatment.


Dysplasia epiphysealis capitis femoris Hip Legg-Calvé-Perthes disease Meyer dysplasia

This content is not available in html format but you may download it in Acrobat Reader (PDF).


This article has no comments yet.