Ehlers-Danlos syndrome, musculocontractural variant. A case report

Ehlers-Danlos syndrome comprises a group of hereditary disordes that share skin hyperextensibility, joint hipermobility and tissular fragility manifested as diminished tensile strenght and integrity of skin and joints. The estimated frequency, for the whole group, is 1 in 5.000 to 1 in 10.000 people...

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Bibliographic Details
Main Authors: Franco-Buenaventura, Daniela, Ramírez-Cheyne, Julián, Saldarriaga-Gil, Wilmar
Format: Article
Language:Spanish
Published: Universidad de Antioquia 2016-07-01
Series:Iatreia
Subjects:
Online Access:http://aprendeenlinea.udea.edu.co/revistas/index.php/iatreia/article/view/23708/20780567