Clinical and Genetic Features of Vascular Ehlers-Danlos Syndrome
β Scribed by Dominique P. Germain
- Publisher
- Springer
- Year
- 2002
- Tongue
- English
- Weight
- 120 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0890-5096
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Ehlers-Danlos syndrome (EDS) type IV is a clinically and genetically heterogeneous disorder characterized by thin skin, prominent venous vascular markings, markedly increased bruising, and an increased likelihood of large bowel and large artery rupture. We studied two type IV EDS patients. Both have
## Abstract ## Objective To demonstrate the high frequency and lack of diagnosis of joint hypermobility syndrome (JHS) and the seriousness of vascular EhlersβDanlos syndrome (VEDS). ## Methods Two hundred fortyβnine Chilean patients with hereditary disorders of the connective tissues (CTDs) and