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| | eMedicine - Marfan Syndrome : Article by Khalid Channell, MD (Site not responding. Last check: 2007-10-20) |
 | | The skeleton typically displays multiple deformities including arachnodactyly (ie, abnormally long and thin digits), dolichostenomelia (ie, long limbs relative to trunk length), pectus deformities (ie, excavatum and carinatum), and thoracolumbar scoliosis. |
 | | In later studies, further anomalies were documented, including arachnodactyly (long digits), cardiovascular abnormalities, and dislocation of the ocular lens. |
 | | A common and often lethal complication is dissection of the aorta, and inheritance is now known to be autosomal. |
| www.emedicine.com /orthoped/topic414.htm (4091 words) |
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