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Ehlers Danlos Syndrome – A Case Report

Identifieur interne : 000824 ( Main/Merge ); précédent : 000823; suivant : 000825

Ehlers Danlos Syndrome – A Case Report

Auteurs : Pragati Kaurani ; Nikhil Marwah ; Mayank Kaurani ; Narendra Padiyar

Source :

Journal of Clinical and Diagnostic Research : JCDR [ 2249-782X ] ; 2014.

RBID : PMC:4003659

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:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003659

DOI: 10.7860/JCDR/2014/4569.4178
PubMed: 24783151
PubMed Central: 4003659

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PMC:4003659

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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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Ehlers Danlos Syndrome – A Case Report

Ehlers Danlos Syndrome – A Case Report

Source :

Abstract

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