Literature DB >> 7802002

Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients.

K Elbedour1, N Zucker, E Zalzstein, Y Barki, R Carmi.   

Abstract

The Bardet-Biedl syndrome is an autosomal recessive disorder of polydactyly, obesity, tapetoretinal degeneration, mental retardation, hypogenitalism, and renal involvement. A high incidence of congenital and acquired heart disease was reported in the former "Laurence-Moon-Biedl-Bardet" syndrome. However, since the establishment of the Bardet-Biedl syndrome as a separate clinical entity, cardiac involvement has not been evaluated in this disorder. We have performed echocardiographic studies on 22 patients with the Bardet-Biedl syndrome from three extended, highly inbred Bedouin families. In addition to previously reported congenital heart defects we have observed hypertrophy of the interventricular septum and dilated cardiomyopathy. Our findings of cardiac involvement in 50% of the cases suggest that echocardiographic examination should be included in the clinical evaluation and follow-up of patients with Bardet-Biedl syndrome.

Entities:  

Mesh:

Year:  1994        PMID: 7802002     DOI: 10.1002/ajmg.1320520208

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  31 in total

Review 1.  Molecular basis of the obesity associated with Bardet-Biedl syndrome.

Authors:  Deng-Fu Guo; Kamal Rahmouni
Journal:  Trends Endocrinol Metab       Date:  2011-04-21       Impact factor: 12.015

2.  Management of a 10-month-old child with a rare combination of Bardet-Biedl syndrome and ano-rectal malformation undergoing anterior sagittal ano-rectoplasty.

Authors:  Harihar V Hegde; Rohini Bhat Pai; Vijay G Yaliwal; Venkatesh M Annigeri; Anil B Halgeri; P Raghavendra Rao
Journal:  J Anesth       Date:  2011-10-15       Impact factor: 2.078

3.  Bardet-Biedl syndrome.

Authors:  Elizabeth Forsythe; Philip L Beales
Journal:  Eur J Hum Genet       Date:  2012-06-20       Impact factor: 4.246

4.  Bardet-Biedl syndrome: a study of the renal and cardiovascular phenotypes in a French cohort.

Authors:  Olivier Imhoff; Vincent Marion; Corinne Stoetzel; Myriam Durand; Muriel Holder; Sabine Sigaudy; Pierre Sarda; Christian P Hamel; Christian Brandt; Hélène Dollfus; Bruno Moulin
Journal:  Clin J Am Soc Nephrol       Date:  2010-09-28       Impact factor: 8.237

5.  Smooth Muscle Cell-Specific Disruption of the BBSome Causes Vascular Dysfunction.

Authors:  John J Reho; Deng-Fu Guo; Donald A Morgan; Kamal Rahmouni
Journal:  Hypertension       Date:  2019-08-19       Impact factor: 10.190

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

Authors:  Annie P Chiang; Darryl Nishimura; Charles Searby; Khalil Elbedour; Rivka Carmi; Amanda L Ferguson; Jenifer Secrist; Terry Braun; Thomas Casavant; Edwin M Stone; Val C Sheffield
Journal:  Am J Hum Genet       Date:  2004-07-16       Impact factor: 11.025

7.  Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning.

Authors:  Marwan K Tayeh; Hsan-Jan Yen; John S Beck; Charles C Searby; Trudi A Westfall; Hilary Griesbach; Val C Sheffield; Diane C Slusarski
Journal:  Hum Mol Genet       Date:  2008-04-01       Impact factor: 6.150

8.  Bardet-Biedl syndrome: multiple fingers with multiple defects!

Authors:  Jagadesh Madireddi; Vasuveda Acharya; Jandhyala Suryanarayana; Handattu Manjunath Hande; Ranjan Shetty
Journal:  BMJ Case Rep       Date:  2015-11-26

9.  Day care general anaesthesia for a child with bardet-biedl syndrome.

Authors:  Suresh Chittoodan; Suzanne Crowe
Journal:  Case Rep Med       Date:  2010-08-01

10.  Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform.

Authors:  Pamela R Pretorius; Lisa M Baye; Darryl Y Nishimura; Charles C Searby; Kevin Bugge; Baoli Yang; Robert F Mullins; Edwin M Stone; Val C Sheffield; Diane C Slusarski
Journal:  PLoS Genet       Date:  2010-03-19       Impact factor: 5.917

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