Ehlers-Danlos Syndrome
A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.
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Subheadings:
Tree Number(s): C14.907.454.240, C15.378.463.515.240, C16.131.831.428, C16.320.850.260, C17.300.200.310, C17.800.804.428, C17.800.827.260
MeSH Unique ID: D004535
Entry Terms:
- Ehlers Danlos Syndrome
- Syndrome, Ehlers-Danlos
- Ehlers-Danlos Disease
- Disease, Ehlers-Danlos
- Cutis Elastica
- Ehlers Danlos Disease
- Danlos Disease, Ehlers
- Disease, Ehlers Danlos
See Also: