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
β¦ LIBER β¦
The spectrum, management and clinical outcome of Ehlers-Danlos syndrome type IV: A 30-year experience
β Scribed by Oderich, Gustavo S.; Panneton, Jean M.; Bower, Thomas C.; Lindor, Noralane M.; Cherry, Kenneth J.; Noel, Audra A.; Kalra, Manju; Sullivan, Timothy; Gloviczki, Peter
- Book ID
- 122332447
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 280 KB
- Volume
- 42
- Category
- Article
- ISSN
- 1097-6809
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