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IP International Journal of Ocular Oncology and Oculoplasty


A case report: Bardet-Biedle syndrome


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Author Details : Girjesh Kain, Megha Srivastava, Mamta Kumari

Volume : 3, Issue : 4, Year : 2017

Article Page : 321-323


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Abstract

Bardet-Biedle syndrome is an autosomal recessive disorder named after George Bardet & Arthur Biedle. Bardet-Biedle syndrome is characterized by rods-cones dystrophy, truncal obesity, postaxial polyductyly, cognitive impairment, male hypogonadism, and renal abnormalities. The purpose of this article is to provide detailed review of Bardet-Biedle syndrome.

Keywords:­ Bardet-Biedle Syndrome, Retinitis Pigmentosa, Rods-cones dystrophy.

How to cite : Kain G, Srivastava M, Kumari M, A case report: Bardet-Biedle syndrome. IP Int J Ocul Oncol Oculoplasty 2017;3(4):321-323

Copyright © 2017 by author(s) and IP Int J Ocul Oncol Oculoplasty. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (creativecommons.org)