| Literature DB >> 24179926 |
Rupal V Dosi1, Nikita R Bhatt, Annirudh P Ambaliya, Nitin N Sonune, Rushad D Patell.
Abstract
Bardet Biedel Syndrome (BBS) is a rare autosomal recessive disease which is characterized by obesity, retinitis pigmentosa, polydactyly, neuro-developmental retardation and renal defects amongst others. It is a genetically heterogeneous ciliopathic disorder with inter and intra familial variations. Very few cases have been reported from India. We are reporting here a case of an adolescent girl who was diagnosed at the age of 16, with additional features of insulin resistance and non-alcoholic fatty liver disease. A review of recent literature and a short discussion on the care and management of this uncommon condition follow.Entities:
Keywords: Bardet Biedel Syndrome; Obesity; Retinitis pigmentosa
Year: 2013 PMID: 24179926 PMCID: PMC3809665 DOI: 10.7860/JCDR/2013/5684.3388
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X