Literature DB >> 35103156

Bardet-Biedl Syndrome With Renal, Cardiac, and Genitourinary Malformations: A Case Report.

Madeeha Subhan Waleed1, Ashok Abraham Varughese2, Vineeth Amba3, Radhika Pathalapati4.   

Abstract

Bardet-Biedl syndrome (BBS), also known as Laurence-Moon-Bardet-Biedl syndrome, is a unique autosomal recessive genetic disorder that involves multiple organ systems with an incidence under 1/100,000 in Europe and the USA. We present a case of a 27-year-old male with BBS and a past medical history of hypertension. He was diagnosed with BBS when he was a child. His physical examination showed polydactyly in the feet. His renal ultrasound showed the left kidney with a double collecting system and measured 1.9 × 6.1 × 3.6 cm and extended from the left upper quadrant to the left lower quadrant. His CT of the abdomen showed a horseshoe-shaped kidney with right moiety. Renal abnormalities in BBS have been identified recently. BBS is also associated with various cardiac manifestations such as patent ductus arteriosus, cardiomyopathies, and valvular diseases. BBS requires multidisciplinary management and a close follow-up with a nephrologist to decrease morbidity and mortality. Genetic and molecular mapping of this disorder will aid the understanding of congenital renal ciliopathies.
Copyright © 2021, Waleed et al.

Entities:  

Keywords:  bardet-biedl syndrome; horse shoe kidney; laurence-moon-bardet-biedl syndrome; mitral valve replacement; renal pathology

Year:  2021        PMID: 35103156      PMCID: PMC8776535          DOI: 10.7759/cureus.20577

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


  7 in total

1.  Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families.

Authors:  P L Beales; A M Warner; G A Hitman; R Thakker; F A Flinter
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

2.  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

3.  Focal and segmental glomerulosclerosis and porteinuria associated with unilateral renal agenesis.

Authors:  D D Kiprov; R B Colvin; R T McCluskey
Journal:  Lab Invest       Date:  1982-03       Impact factor: 5.662

Review 4.  Making sense of cilia in disease: the human ciliopathies.

Authors:  Kate Baker; Philip L Beales
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

5.  Congenital renal abnormalities in the Laurence-Moon-Biedl syndrome.

Authors:  N H Bluett; C Chantler; J D Singer; H M Saxton
Journal:  Arch Dis Child       Date:  1977-12       Impact factor: 3.791

6.  Risk Factors for Severe Renal Disease in Bardet-Biedl Syndrome.

Authors:  Elizabeth Forsythe; Kathryn Sparks; Sunayna Best; Sarah Borrows; Bethan Hoskins; Ataf Sabir; Timothy Barrett; Denise Williams; Shehla Mohammed; David Goldsmith; David V Milford; Detlef Bockenhauer; Lukas Foggensteiner; Philip L Beales
Journal:  J Am Soc Nephrol       Date:  2016-09-22       Impact factor: 10.121

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

Authors:  Laila Tul Qadar; Zohaib M Ahmed; Maham Munawar; Choudhary A Hasan; Syed Umair Iqbal
Journal:  Cureus       Date:  2019-06-11
  7 in total

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