Literature DB >> 9415685

Brachydactyly-short stature-hypertension (Bilginturan) syndrome: report on two families.

D Chitayat1, A Grix, J W Balfe, J S Abramowicz, J Garza, C T Fong, M M Silver, D N Saller, G H Bresnick, A Giedion, R S Lachman, D L Rimoin.   

Abstract

We report on two families with autosomal dominant brachydactyly of hands and feet and hypertension. All affected members of the first family had proportionate short stature. However, the propositus and the affected relatives in the second family were only short compared to unaffected relatives. The hypertension was medically responsive in all cases. The propositus in the second family had poor compliance and a striking generalized vasculopathy. All patients were of normal intelligence and had a normal facial appearance. The brachydactyly-short stature-hypertension syndrome was first reported by Bilginturan et al. [1973] in a Turkish family and the families reported by us are Caucasian and Hispanic. The gene causing this condition in the original Turkish family was recently mapped to 12p. Our report expands our existing knowledge and the ethnic diversity of this syndrome.

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Year:  1997        PMID: 9415685     DOI: 10.1002/(sici)1096-8628(19971219)73:3<279::aid-ajmg10>3.0.co;2-g

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


  2 in total

1.  Brachydactyly short-stature hypertension syndrome: a case with associated vascular malformations.

Authors:  Murat Derbent; Esra Baskin; Muhteşem Ağildere; Pinar Isik Agras; Umit Saatçi
Journal:  Pediatr Nephrol       Date:  2005-12-21       Impact factor: 3.714

Review 2.  Brachydactyly E: isolated or as a feature of a syndrome.

Authors:  Arrate Pereda; Intza Garin; Maria Garcia-Barcina; Blanca Gener; Elena Beristain; Ane Miren Ibañez; Guiomar Perez de Nanclares
Journal:  Orphanet J Rare Dis       Date:  2013-09-12       Impact factor: 4.123

  2 in total

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