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Clinical and Genetic Features of Vascular Ehlers-Danlos Syndrome

✍ 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

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## Abstract ## Objective To demonstrate the high frequency and lack of diagnosis of joint hypermobility syndrome (JHS) and the seriousness of vascular Ehlers‐Danlos syndrome (VEDS). ## Methods Two hundred forty‐nine Chilean patients with hereditary disorders of the connective tissues (CTDs) and