Literature DB >> 2773990

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

E A Haan1, Y J Hull, S White, R Cockington, P Charlton, D F Callen.   

Abstract

Here we report on a family with an inherited rearrangement of chromosome 8q, dir ins(8)(q24.11q13.3q21.13). Individuals with the chromosome abnormality, which does not appear to be associated with deletion of chromosome material, have manifestations of both tricho-rhino-phalangeal syndrome (TRPS) and branchio-oto syndrome (BOS). TRPS has been linked previously to deletions involving 8q24.11----q24.13, but none of the described patients with deletions in this part of 8q have had characteristics of the BOS. The presence of a breakpoint in 8q24.11 without apparent chromosome deletion in the family described suggests that TRPS maps to this band of 8q. Further, it is suggested that BOS maps to either 8q13.3 or 8q21.13.

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Year:  1989        PMID: 2773990     DOI: 10.1002/ajmg.1320320412

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


  10 in total

1.  A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type I.

Authors:  T Sasaki; H Tonoki; H Soejima; N Niikawa
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome.

Authors:  Amarilis Sanchez-Valle; Xueqing Wang; Lorraine Potocki; Zhilian Xia; Sung-Hae L Kang; Mary E Carlin; Donnice Michel; Patricia Williams; Gerardo Cabrera-Meza; Ellen K Brundage; Anna L Eifert; Pawel Stankiewicz; Sau Wai Cheung; Seema R Lalani
Journal:  Am J Med Genet A       Date:  2010-11       Impact factor: 2.802

3.  Urinary tract abnormalities (UTA) and associated malformations: data of the Emilia-Romagna Registry. IMER Group. Emilia-Romagna Registry on Congenital Malformations.

Authors:  G Cocchi; C Magnani; M S Morini; G P Garani; M Milan; E Calzolari
Journal:  Eur J Epidemiol       Date:  1996-10       Impact factor: 8.082

Review 4.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

Review 5.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

6.  1992 American Society of Human Genetics presidential address: back to the future.

Authors:  W E Nance
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

7.  Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree.

Authors:  R König; S Fuchs; C Dukiet
Journal:  Eur J Pediatr       Date:  1994-06       Impact factor: 3.183

8.  Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.

Authors:  S Kumar; W J Kimberling; C J Connolly; S Tinley; H A Marres; C W Cremers
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

9.  Non-inherited manifestation of bilateral branchial fistulae, bilateral pre-auricular sinuses and bilateral hearing loss: A variant of branchio-oto-renal syndrome.

Authors:  Indu Rana; Rajiv Dhawan; Sanjay Gudwani; Rajendra Bothra; N N Mathur
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2005-01

10.  From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report.

Authors:  Elena Cacciatori; Sebastiano Aleo; Giulietta Scuvera; Chiara Rigon; Paola Giovanna Marchisio; Matteo Cassina; Donatella Milani
Journal:  Ital J Pediatr       Date:  2022-10-01       Impact factor: 3.288

  10 in total

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