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Marfan Syndrome in an Iranian Family: A Case Series | ||
| Iranian Journal of Medical Sciences | ||
| مقاله 11، دوره 39، شماره 4، مهر 2014، صفحه 391-394 اصل مقاله (931.5 K) | ||
| نوع مقاله: Case Report(s) | ||
| نویسندگان | ||
| Mohammad Hossein Davari؛ Toba Kazemi* | ||
| Birjand Atherosclerosis and Coronary Artery Research Centre, Birjand University of Medical Sciences, Birjand, Iran | ||
| چکیده | ||
| Marfan syndrome (MFS) is a genetic disorder which is inherited by autosomal dominant traits. In MFS, lens displacement and cardiovascular involvement are important causes of morbidity and mortality in the clinical course of the disease. In this case study, the ocular involvement in a family with severe penetration of MFS is reported. Twelve members of a family (father, two daughters, three sons, and six grandchildren) had MFS. Lens ectopia was the most common ophthalmic involvement among the family (100%). Other ocular involvements were as follows; Hypoplastic iris or ciliary’s muscle hypoplasia (50%), on gated eyeball (42%), flat cornea (30%), glaucoma and cataract (25%), retinal detachment (16%). Three members of the family underwent eye surgery including lens extraction, glaucoma surgery and retinal surgery. | ||
| کلیدواژهها | ||
| Marfan syndrome؛ Eye Manifestations؛ Ectopia Lentis | ||
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آمار تعداد مشاهده مقاله: 2,996 تعداد دریافت فایل اصل مقاله: 1,145 |
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