Ehlers–Danlos syndrome: case report and an electron microscopy study

Ehlers–Danlos syndrome (EDS) type III is a inherited connective tissue disorders characterized by extensibility of the skin, hypermobility of the joints, chronic pain, tissue fragility, easy bruising, and delayed wound healing with result of atrophic scars. The patients report commonly a history of...

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Veröffentlicht in:	Rheumatology international 2012-06, Vol.32 (6), p.1507-1510
Hauptverfasser:	Carlesimo, M., Cortesi, G., Gamba, A., Narcisi, A., Turturro, F., Raffa, S., Torrisi, M. R., Camplone, G.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biopsy Dermis - ultrastructure Ehlers-Danlos Syndrome - complications Ehlers-Danlos Syndrome - diagnosis Ehlers-Danlos Syndrome - genetics Ehlers-Danlos Syndrome - pathology Female Fibrillar Collagens - ultrastructure Humans Joint Dislocations - etiology Joint Instability - etiology Medicine Medicine & Public Health Microscopy, Electron, Transmission Middle Aged Original Article Predictive Value of Tests Recurrence Rheumatology
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