Literature DB >> 20949666

Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity.

Julie C Sapp1, Darryl Nishimura, Jennifer J Johnston, Edwin M Stone, Elise Héon, Val C Sheffield, Leslie G Biesecker.   

Abstract

PURPOSE: Bardet-Biedl syndrome is a pleiotropic multiple anomaly syndrome inherited in an autosomal recessive pattern. It is now known that this disorder has locus heterogeneity, with causative mutations identified in as many as 14 genes. The aim of this study was to derive locus-specific recurrence risk estimates for family members of a proband affected with Bardet-Biedl syndrome.
METHODS: Mutation data from 187 probands affected with Bardet-Biedl syndrome were used. The authors counted the relative proportion of families with mutations at each of 10 loci and estimated locus-specific carrier rates for mutations using Hardy-Weinberg principles and an aggregate population frequency of 1/100,000 for the phenotype. Locus-specific recurrence risks were calculated for relatives of an affected proband.
RESULTS: Locus-specific carrier frequencies range from 1/250 to 1/2200, and the risks for an offspring of the sibling of an affected individual range from 1/1,500 to 1/13,000. The estimate of this risk derived under a locus homogeneity model is 1/960.
CONCLUSION: Variation of recurrence risks of this magnitude may have implications for genetic counseling of families with affected individuals, in particular about prenatal testing and other reproductive options. Similar analyses to determine locus-specific carrier frequencies for other phenotypes with significant locus heterogeneity may yield similarly relevant results.

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Year:  2010        PMID: 20949666      PMCID: PMC3115203          DOI: 10.1097/GIM.0b013e3181f07572

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  20 in total

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5.  Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene.

Authors:  Darryl Y Nishimura; Ruth E Swiderski; Charles C Searby; Erik M Berg; Amanda L Ferguson; Raoul Hennekam; Saul Merin; Richard G Weleber; Leslie G Biesecker; Edwin M Stone; Val C Sheffield
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6.  Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

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8.  Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3).

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9.  Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.

Authors:  José L Badano; Stephen J Ansley; Carmen C Leitch; Richard Alan Lewis; James R Lupski; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2003-02-03       Impact factor: 11.025

10.  BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.

Authors:  Corinne Stoetzel; Virginie Laurier; Erica E Davis; Jean Muller; Suzanne Rix; José L Badano; Carmen C Leitch; Nabiha Salem; Eliane Chouery; Sandra Corbani; Nadine Jalk; Serge Vicaire; Pierre Sarda; Christian Hamel; Didier Lacombe; Muriel Holder; Sylvie Odent; Susan Holder; Alice S Brooks; Nursel H Elcioglu; Eduardo D Silva; Eduardo Da Silva; Béatrice Rossillion; Sabine Sigaudy; Thomy J L de Ravel; Richard Alan Lewis; Bruno Leheup; Alain Verloes; Patrizia Amati-Bonneau; André Mégarbané; Olivier Poch; Dominique Bonneau; Philip L Beales; Jean-Louis Mandel; Nicholas Katsanis; Hélène Dollfus
Journal:  Nat Genet       Date:  2006-04-02       Impact factor: 38.330

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4.  Cognitive, sensory, and psychosocial characteristics in patients with Bardet-Biedl syndrome.

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5.  Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing.

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Journal:  Cell J       Date:  2018-03-18       Impact factor: 2.479

6.  Laurence-Moon-Bardet-Biedl Syndrome with Coexisting Abdominal Distension and Positive Fluid Thrill: A Rare Manifestation Reported in Karachi, Pakistan.

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