DR. SANJAY BOSAK

DR. TANMAY SRIVASTAV, DR. KALYAN SINGH MAURYA, DR. DEEPAK MISHRA

Abstract

Purpose:Marfan syndrome is an autosomal dominant multi systemic disorder of the connective tissue occurringin 8-10 per 100,000 of population/year. Purpose of this case report was to demonstrate the ocular and systemic characteristics in 17year female.Methods:The patient presented with complaints of diminution in vision both eyes since childhood. The patient underwentdetailed general examination, complete ophthalmic examination including vision, slit lamp, fundus andother radiological and cardiovascular investigations.Results:General examination revealed tall thin stature along with long and thin extremities,elongated fingers and toes, high-arched palate.On ocular examination inferonasal subluxation of lens was found in right eye and supero-temporal subluxation of lens was found in left eye.Conclusion: On the basis of examination she was diagnosed with Marfan syndrome.Early detection of this condition and associated complications are required to reduce associated ophthalmic problems.