NALT

Preferred term

Ehlers Danlos syndrome

Topic

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.

cutis elastica

Field 001 in MARC Authority Format

95085

Spanish

síndrome de Ehlers-Danlos

URI

https://lod.nal.usda.gov/nalt/335757

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Created 1/31/20, last modified 10/29/20