Intercalary staphyloma in Marfan syndrome: A dreaded complication of scleral incision
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چکیده
منابع مشابه
Marfan Syndrome in an Iranian Family: A Case Series
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...
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A 22 year old male referred with palpitation. General appearance and physical exam impressed us in that the patient has Marfan syndrome. Cardiac catheterization showed diffuse arterial ectasia. We found no previous report of this generalized diffuse ectasia.
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ژورنال
عنوان ژورنال: Indian Journal of Ophthalmology
سال: 2019
ISSN: 0301-4738
DOI: 10.4103/ijo.ijo_1672_18