Bardet-Biedl Syndrome: A Rare Entity

Bardet-Biedl syndrome (BBS) is a rare ciliopathy autosomal recessive hereditary disorder due to mutation in 14 genes. It affects multiple organ systems such as renal dysfunction, congenital heart disease, ocular defect, cognitive impairment, and speech disorder and presented clinically as truncal ob...

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Bibliographic Details
Main Authors: Anuja Goit, Sonal Gupta, Shilpi Dutta
Format: Article
Language:English
Published: Jaypee Brothers Medical Publisher 2022-08-01
Series:Journal of South Asian Association of Pediatric Dentistry
Subjects:
Online Access:https://www.jsaapd.com/doi/JSAAPD/pdf/10.5005/jp-journals-10077-3224
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