Ehlers-Danlos syndrome
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Ehlers-Danlos syndrome is a syndrome due to a genetic defect.
Features:[1]
- Atrial rupture.
- Intestina rupture.
- Uterine rupture.
- Easy bruising.
- Characteristic facies.
Incidence
- 1 in 5000.[1]
See also
References
- ↑ 1.0 1.1 Jarmulowicz M, Phillips WG (January 2001). "Vascular Ehlers-Danlos syndrome undiagnosed during life". J R Soc Med 94 (1): 28–30. PMC 1280067. PMID 11220066. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280067/pdf/11220066.pdf.