Condition
Ehlers-Danlos Syndrome
Dermatology
Overview
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.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Ehlers-Danlos Syndrome
- Topic type
- Condition
- Category
- Dermatology
- MeSH classification
- 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
Preparing for an appointment about Ehlers-Danlos Syndrome
If you are speaking with a healthcare professional about Ehlers-Danlos Syndrome, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to Ehlers-Danlos Syndrome
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Clinics related to Ehlers-Danlos Syndrome
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.