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FP0006 : A RARE CASE OF ALPORT SYNDROME

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FP0006 : A RARE CASE OF ALPORT SYNDROME

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Chief & Presenting Author: Dr.Snehal Rajgire

Co Author(s): Dr.Dr Nikhilesh Anil Wairagade

Abstract

We present the case of 20 years old male presented by his parents to OPD with chief complaints of OU diminution of vision. The parents also notices impaired hearing and generalized weakness. On further evaluation, he had history of kidney disorder under management with secondary hypertension. Family history was negative suggestive of autosomal recessive. On examination, BCVA was OD 4/60- 6/18, OS 3/60-6/36 with myopic astigmatism on snellens chart. Anterior segment reveals clear cornea with anterior lenticonus . On retinoscopy scissoring reflex was present. Fundus was normal. On OCT – normal foveal contour, ASOCT and pentacam was normal. He was advised clear lens extraction with IOL and ENT specialist opinion for hearing loss, nephrologist opinion in view of kidney transplantation. Patient was diagnosed with triad – Anterior lenticonus , kidney disorder and hearing loss.

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