Literature DB >> 22109794

Prevalence of Bardet-Biedl syndrome in Tunisia.

Oussama M'hamdi1, Ines Ouertani, Faouzi Maazoul, Habiba Chaabouni-Bouhamed.   

Abstract

Bardet-Biedl syndrome (BBS, OMIM 209900) is a ciliopathy causing multivisceral abnormalities. This disease is mainly characterized by obesity, post-axial polydactyly, hypogenitalism, intellectual disabilities, pigmentary retinopathy, and renal deficiency. The prevalence of BBS has been estimated in different populations, ranging from 1 in 160,000 in European populations to 1 in 13,000 in Bedouins from Kuwait. In the present report, we present the first epidemiological study of Bardet-Biedl syndrome in Tunisia. From 1984 to 2009, 46 Tunisian families, including 67 affected members, were diagnosed as BBS. The patients' ages ranged between 6 months and 37 years, with median age of 10.4 years. High level of consanguinity was noted in our cohort (93.47%). The overall minimum prevalence in our population was estimated to be approximately 1 in 156,000 individuals. Our study reflects the actual frequency of BBS in North Africa and showed that this disease seems uncommon.

Entities:  

Year:  2011        PMID: 22109794      PMCID: PMC3186025          DOI: 10.1007/s12687-011-0040-6

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  10 in total

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10.  Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alström syndrome.

Authors:  Ines Pereiro; Bethan E Hoskins; Jan D Marshall; Gayle B Collin; Jürgen K Naggert; Teresa Piñeiro-Gallego; Eneli Oitmaa; Nicholas Katsanis; Diana Valverde; Philip L Beales
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  10 in total
  11 in total

1.  Mutation profile of BBS genes in Iranian patients with Bardet-Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes.

Authors:  Zohreh Fattahi; Parvin Rostami; Amin Najmabadi; Marzieh Mohseni; Kimia Kahrizi; Mohammad Reza Akbari; Ariana Kariminejad; Hossein Najmabadi
Journal:  J Hum Genet       Date:  2014-05-22       Impact factor: 3.172

Review 2.  Bardet-Biedl Syndrome.

Authors:  Evgeny N Suspitsin; Evgeny N Imyanitov
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Review 3.  Update on the genetics of bardet-biedl syndrome.

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4.  Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.

Authors:  Kentaro Kurata; Katsuhiro Hosono; Akiko Hikoya; Akihiko Kato; Hirotomo Saitsu; Shinsei Minoshima; Tsutomu Ogata; Yoshihiro Hotta
Journal:  Jpn J Ophthalmol       Date:  2018-04-17       Impact factor: 2.447

5.  Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye.

Authors:  Katie Weihbrecht; Wesley A Goar; Thomas Pak; Janelle E Garrison; Adam P DeLuca; Edwin M Stone; Todd E Scheetz; Val C Sheffield
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6.  Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.

Authors:  Dong-Jun Xing; Hong-Xing Zhang; Na Huang; Kun-Chao Wu; Xiu-Feng Huang; Fang Huang; Yi Tong; Chi-Pui Pang; Jia Qu; Zi-Bing Jin
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7.  Genetics and genomic medicine in Tunisia.

Authors:  Houda Elloumi-Zghal; Habiba Chaabouni Bouhamed
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8.  Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families.

Authors:  Susan Akbaroghli; Daniz Kooshavar; Zahra Golchehre; Arezou Karamzade; Mohammad Saberi; Mohammad Reza Alaei; Masoud Abbasi Sadegh; Mostafa Asadollahi; Mohammad Keramatipour
Journal:  Iran J Child Neurol       Date:  2022-01-01

9.  Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.

Authors:  Muzammil Ahmad Khan; Sumitra Mohan; Muhammad Zubair; Christian Windpassinger
Journal:  BMC Med Genet       Date:  2016-02-04       Impact factor: 2.103

10.  Novel homozygous protein-truncating mutation of BBS9 identified in a Chinese consanguineous family with Bardet-Biedl syndrome.

Authors:  Hai-Yan Tang; Fen Xie; Ru-Chun Dai; Xiao-Liu Shi
Journal:  Mol Genet Genomic Med       Date:  2021-07-02       Impact factor: 2.183

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