Literature DB >> 28511423

Bardet Biedl Syndrome - A Report of Two Cases with Otolaryngologic Symptoms.

Mahendra K Singh1, Sidharth Pradhan2, Priyanko Chakraborty2.   

Abstract

Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive disorder characterized primarily by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, hypogonadism, and renal dysfunction. We present two cases of this syndrome, both female, who presented with complaints of nyctalopia and mental retardation, and additionally one of them had sensorineural hearing loss while the other had serous otitis media. Hearing loss being a rare presentation is worth reporting. Both the patients were given a course of vitamin A and the parents were counseled regarding the prognosis and additional complications associated with the syndrome.

Entities:  

Keywords:  Hearing loss; Postaxial polydactyly; Rod-cone dystrophy; Serous otitis media

Year:  2017        PMID: 28511423      PMCID: PMC5427349          DOI: 10.7860/JCDR/2017/24499.9466

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  7 in total

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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

2.  Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.

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Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

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Authors:  J Z Laurence; R C Moon
Journal:  Obes Res       Date:  1995-07

4.  Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

Authors:  M Leppert; L Baird; K L Anderson; B Otterud; J R Lupski; R A Lewis
Journal:  Nat Genet       Date:  1994-05       Impact factor: 38.330

5.  Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping.

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Journal:  Hum Mol Genet       Date:  1994-08       Impact factor: 6.150

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Authors:  R Carmi; T Rokhlina; A E Kwitek-Black; K Elbedour; D Nishimura; E M Stone; V C Sheffield
Journal:  Hum Mol Genet       Date:  1995-01       Impact factor: 6.150

7.  The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome.

Authors:  J S Green; P S Parfrey; J D Harnett; N R Farid; B C Cramer; G Johnson; O Heath; P J McManamon; E O'Leary; W Pryse-Phillips
Journal:  N Engl J Med       Date:  1989-10-12       Impact factor: 91.245

  7 in total
  1 in total

1.  NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases.

Authors:  I Perea-Romero; F Blanco-Kelly; I Sanchez-Navarro; I Lorda-Sanchez; S Tahsin-Swafiri; A Avila-Fernandez; I Martin-Merida; M J Trujillo-Tiebas; R Lopez-Rodriguez; M Rodriguez de Alba; I F Iancu; R Romero; M Quinodoz; H Hakonarson; Blanca Garcia-Sandova; P Minguez; M Corton; C Rivolta; C Ayuso
Journal:  Hum Genet       Date:  2021-08-26       Impact factor: 4.132

  1 in total

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