Ehlers Danlos Syndrome – A Case Report
Identifieur interne : 000822 ( Main/Exploration ); précédent : 000821; suivant : 000823Ehlers Danlos Syndrome – A Case Report
Auteurs : Pragati Kaurani ; Nikhil Marwah ; Mayank Kaurani ; Narendra PadiyarSource :
- Journal of Clinical and Diagnostic Research : JCDR [ 2249-782X ] ; 2014.
Abstract
Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.
Url:
DOI: 10.7860/JCDR/2014/4569.4178
PubMed: 24783151
PubMed Central: 4003659
Affiliations:
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<front><div type="abstract" xml:lang="en"><p>Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.</p>
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