Case Report
Author Details :
Volume : 3, Issue : 4, Year : 2017
Article Page : 321-323
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
This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
Viewed: 2672
PDF Downloaded: 1532