Literature DB >> 24179926

Bardet biedel syndrome: a very rare entity in India.

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


  5 in total

1.  Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.

Authors:  Stephen J Ansley; Jose L Badano; Oliver E Blacque; Josephine Hill; Bethan E Hoskins; Carmen C Leitch; Jun Chul Kim; Alison J Ross; Erica R Eichers; Tanya M Teslovich; Allan K Mah; Robert C Johnsen; John C Cavender; Richard Alan Lewis; Michel R Leroux; Philip L Beales; Nicholas Katsanis
Journal:  Nature       Date:  2003-09-21       Impact factor: 49.962

2.  Laurence-Moon-Bardet-Biedl syndrome.

Authors:  J K Sahu; V Jain
Journal:  JNMA J Nepal Med Assoc       Date:  2008 Oct-Dec       Impact factor: 0.406

3.  Bardet-Biedl syndrome: a rare case report from North India.

Authors:  Sumir Kumar; Bharat B Mahajan; Jyotisterna Mittal
Journal:  Indian J Dermatol Venereol Leprol       Date:  2012 Mar-Apr       Impact factor: 2.545

4.  New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.

Authors:  P L Beales; N Elcioglu; A S Woolf; D Parker; F A Flinter
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

Review 5.  Recent advances in the molecular pathology, cell biology and genetics of ciliopathies.

Authors:  M Adams; U M Smith; C V Logan; C A Johnson
Journal:  J Med Genet       Date:  2008-01-04       Impact factor: 6.318

  5 in total

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