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Ehlers-Danlos Syndrome (EDS) type IV. Review of the literature

✍ Scribed by Cristiano Macabu Badauy; Sabrina S. Gomes; Manoel Sant’Ana Filho; José Artur Bogo Chies

Publisher
Springer
Year
2007
Tongue
English
Weight
195 KB
Volume
11
Category
Article
ISSN
1432-6981

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Clinical and ultrastructural heterogenei
Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndrome
✍ Peter H. Byers; Karen A. Holbrook; Barbara McGillivray; Patrick M. MacLeod; R. B 📂 Article 📅 1979 🏛 Springer 🌐 English ⚖ 791 KB

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