Difference between revisions of "Marfan syndrome"
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==See also== | ==See also== | ||
*[[Vascular disease]]. | *[[Vascular disease]]. | ||
*[[Multiple endocrine neoplasia 2B]]. | |||
==References== | ==References== | ||
Revision as of 21:04, 19 March 2011
Marfan syndrome is an autosomal dominant disorder and something vascular surgeons see.
Features - memory device MARFAN:
- Mitral valve prolapse.
- Arachnodactyly (long slender fingers & toes) and other skeletal abnormalities (e.g. pectus excavatum, kyphoscoliosis).
- Retinal detachment.
- Fibrillin-1 defect.[1]
- Aortic aneurysm.
- Neurologic - dural ectasia.[2]
See also
References
- ↑ Cañadas, V.; Vilacosta, I.; Bruna, I.; Fuster, V. (May 2010). "Marfan syndrome. Part 1: pathophysiology and diagnosis.". Nat Rev Cardiol 7 (5): 256-65. doi:10.1038/nrcardio.2010.30. PMID 20351703.
- ↑ URL: http://emedicine.medscape.com/article/946315-overview. Accessed on: 6 September 2010.