Literature DB >> 22604765

Oro-dental findings in Bardet-Biedl syndrome.

Utpal Majumdar1, Gaurav Arya, Santosh Singh, Ajay Pillai, Preeti P Nair.   

Abstract

The Bardet-Biedl syndrome (BBS) is a human genetic disorder with an array of clinical features affecting many body systems. BBS is a pleiotropic disorder with mostly monogenic causes. It is also considered a primary ciliopathy syndrome. It is characterised by obesity, pigmentary retinopathy, polydactyly, mental deficiency and hypogonadism and recently a sixth feature, renal disease, has also been described. Since none of the diverse symptoms of BBS by itself is diagnostic of the disorder and many of the symptoms only become apparent over time, diagnosis of the BBS is often delayed until about 9 years of age when visual problems first appear.

Entities:  

Mesh:

Year:  2012        PMID: 22604765      PMCID: PMC3339191          DOI: 10.1136/bcr.12.2011.5320

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  4 in total

Review 1.  The oligogenic properties of Bardet-Biedl syndrome.

Authors:  Nicholas Katsanis
Journal:  Hum Mol Genet       Date:  2004-02-19       Impact factor: 6.150

2.  Retinal function in carriers of Bardet-Biedl syndrome.

Authors:  Gerald F Cox; Ronald M Hansen; Nicole Quinn; Anne B Fulton
Journal:  Arch Ophthalmol       Date:  2003-06

3.  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

4.  The Laurence-Moon-Biedl-Bardet syndrome. Report of three cases in a Jewish Yemenite family.

Authors:  M Levy; M Lotem; A Fried
Journal:  J Bone Joint Surg Br       Date:  1970-05
  4 in total
  3 in total

Review 1.  Oral and Craniofacial Anomalies of Bardet-Biedl Syndrome: Dental Management in the Context of a Rare Disease.

Authors:  A Panny; I Glurich; R M Haws; A Acharya
Journal:  J Dent Res       Date:  2017-06-29       Impact factor: 6.116

2.  Identification of bone metabolism disorders in patients with Alström and Bardet-Biedl syndromes based on markers of bone turnover and mandibular atrophy.

Authors:  Krzysztof Jeziorny; Ewa Zmyslowska-Polakowska; Krystyna Wyka; Aleksandra Pyziak-Skupień; Maciej Borowiec; Agnieszka Szadkowska; Agnieszka Zmysłowska
Journal:  Bone Rep       Date:  2022-07-01

3.  Bardet-biedl syndrome: a rare cause of chronic kidney disease.

Authors:  Vivek B Kute; Aruna V Vanikar; Manoj R Gumber; Himanshu V Patel; Pankaj R Shah; Sachin B Patil; Hargovind L Trivedi
Journal:  Indian J Clin Biochem       Date:  2012-10-30
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.