Bardet Biedl syndrome – report of a very rare case

Bardet Biedl syndrome – report of a very rare case

Bardet Biedl Syndrome is a autosomal recessive condition with a wide spectrum of clinical features. The principal manifestations of the syndrome are Post axial Polydactyly, Retinitis Pigmentosa, truncal obesity, hypogonadism & renal dysfunction. The authors report a case of Bardet Biedl Syndrome...

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Bibliographic Details
Main Authors: Asha Shirahatti, Daksha Dixit, Harshavardhan Pati
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:National Journal of Clinical Anatomy
Subjects:
bardet biedl syndrome
postaxial polydactyly
retinitis pigmentosa
Online Access:http://www.njca.info/article.asp?issn=2277-4025;year=2016;volume=5;issue=4;spage=228;epage=230;aulast=Shirahatti

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http://www.njca.info/article.asp?issn=2277-4025;year=2016;volume=5;issue=4;spage=228;epage=230;aulast=Shirahatti

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