(3.147.140.12)
Users online: 13611     
Ijournet
Email id
 

Indian Journal of Clinical and Experimental Ophthalmology
Year : 2018, Volume : 4, Issue : 4
First page : ( 554) Last page : ( 555)
Print ISSN : 2395-1443. Online ISSN : 2395-1451.
Article DOI : 10.18231/2395-1451.2018.0124

Bardet- Biedl syndrome – A rare case

Behera Madhusmita1,*, Patra Samir2

1Consultant, Dept. of Oculoplast and Cataract, Rotary Narayana Nethralaya, Kolkata

2Consultant, Ispat General Hospital, Rourkela, Odisha, India

*Corresponding Author: Madhusmita Behera, Email: madhusmita.behera@rediffmail.com

Online published on 14 January, 2019.

Abstract

Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder with wide spectrum of clinical features. BBs is distinguished from the much rarer Laurence-moon syndrome, in which retinal pigmentary degeneration, mental retardation, and hypogonadism occur in association with progressive spastic paraparesis and distal muscle weakness, but without polydactyly. Most common feature of BBS is retinal dystrophy. The visual prognosis for children with Bardet-Biedl syndrome is poor.

Top

Keywords

Mental retardation, Pigmentary retinopathy, Polydactyly.

Top

 
║ Site map ║ Privacy Policy ║ Copyright ║ Terms & Conditions ║ Page Rank Tool
750,843,512 visitor(s) since 30th May, 2005.
All rights reserved. Site designed and maintained by DIVA ENTERPRISES PVT. LTD..
Note: Please use Internet Explorer (6.0 or above). Some functionalities may not work in other browsers.