Literature DB >> 7456592

[The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)].

T Grimm, H Wesselhoeft.   

Abstract

Supravalvular aortic stenosis (SVAS) was seen in 128 families. In 23 families several members had SVAS. In 4 families the Williams-Beuren Syndrome (WBS) was present whereas members of 8 families had some features of the syndrome in addition to their cardiac lesion. In conclusion, no distinct separation can be made between WBS and SVAS. The genetic pattern is autosomal dominant with variable expressivity. The gene frequency is estimated at 10(-4) and the mutation rate at 2.5 . 10(-5).

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Year:  1980        PMID: 7456592

Source DB:  PubMed          Journal:  Z Kardiol        ISSN: 0300-5860


  11 in total

1.  Familial supravalvular aortic stenosis: a genetic study.

Authors:  F Chiarella; F D Bricarelli; G Lupi; P Bellotti; S Domenicucci; C Vecchio
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 2.  Williams syndrome.

Authors:  J Burn
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

3.  Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.

Authors:  Marcy C Speer; David S Enterline; Lorraine Mehltretter; Preston Hammock; Judith Joseph; Margaret Dickerson; Richard G Ellenbogen; Thomas H Milhorat; Michael A Hauser; Timothy M George
Journal:  J Genet Couns       Date:  2003-08       Impact factor: 2.537

4.  Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Authors:  A Mari; F Amati; R Mingarelli; A Giannotti; G Sebastio; V Colloridi; G Novelli; B Dallapiccola
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

5.  A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

Authors:  A K Ewart; C A Morris; G J Ensing; J Loker; C Moore; M Leppert; M Keating
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

6.  Statural growth in Williams-Beuren syndrome.

Authors:  R Pankau; C J Partsch; A Gosch; H C Oppermann; A Wessel
Journal:  Eur J Pediatr       Date:  1992-10       Impact factor: 3.183

7.  De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome.

Authors:  L Telvi; J M Pinard; R Ion; P M Sinet; A Nicole; J Feingold; O Dulac; A Pompidou; G Ponsot
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

8.  Myopathy in Williams-Beuren syndrome.

Authors:  T Voit; H Kramer; C Thomas; W Wechsler; H Reichmann; H G Lenard
Journal:  Eur J Pediatr       Date:  1991-05       Impact factor: 3.183

9.  Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene.

Authors:  A K Ewart; W Jin; D Atkinson; C A Morris; M T Keating
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

10.  Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome.

Authors:  Stefano Stagi; Elisabetta Lapi; Maria Gabriella D'Avanzo; Giancarlo Perferi; Silvia Romano; Sabrina Giglio; Silvia Ricci; Chiara Azzari; Francesco Chiarelli; Salvatore Seminara; Maurizio de Martino
Journal:  BMC Med Genet       Date:  2014-05-23       Impact factor: 2.103

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