Literature DB >> 2918546

Familial supravalvular aortic stenosis: a genetic study.

F Chiarella1, F D Bricarelli, G Lupi, P Bellotti, S Domenicucci, C Vecchio.   

Abstract

Supravalvular aortic stenosis (McKusick 18550) is a rare hereditary condition with autosomal dominant transmission. However, the available data have been limited to small family groups which do not allow the definition of the degree of penetrance of the disease. The present study describes a large family with a high frequency of supravalvular aortic stenosis including five generations and 80 subjects, the largest family group with this disease studied so far. The study was carried out prospectively in 66 subjects (clinical examination, ECG, M mode and two dimensional echocardiography). In 14 subjects available data were examined retrospectively. In 10 patients cardiac catheterisation was performed (prospective study in eight). The disease was present in 36 (45%) of the 80 subjects investigated, on the basis of clinical, echocardiographic, and haemodynamic (when available) criteria. The disease was found to be severe in eight cases (22%), moderate in six cases (17%), mild in 13 (36%), and undefined in eight (22%) patients. In one case (3%), multiple pulmonary stenoses were noted in the absence of supravalvular aortic stenosis. Genetic analysis of these data shows, for the first time, the degree of penetrance of the supravalvular aortic stenosis trait (K = 0.86) and confirms that it is transmitted with incomplete penetrance and variable expressivity.

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Year:  1989        PMID: 2918546      PMCID: PMC1015556          DOI: 10.1136/jmg.26.2.86

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  18 in total

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  4 in total

1.  Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis.

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Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

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Journal:  Pediatr Cardiol       Date:  1992-07       Impact factor: 1.655

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

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Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

4.  Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

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Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

  4 in total

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