Literature DB >> 1952784

Autosomal dominant atrial septal defect of ostium secundum type. Report of three families.

S Li Volti1, G Distefano, R Garozzo, M G Romeo, P Sciacca, F Mollica.   

Abstract

The authors report on three Sicilian families with 17 individuals (10 females and 7 males) in successive generations affected by atrial septal defect of ostium secundum type (S-ASD) without conduction defect. The anomaly was inherited as an autosomal dominant trait. Cytoplasmic inheritance could be excluded, the anomaly being transmitted also by fathers. Familial S-ASD is probably more frequent than commonly reported since cardiological examination of the relatives is not routinely performed in every case of apparently sporadic ASD.

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Year:  1991        PMID: 1952784

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD.

Authors:  Paweł Stańczak; Joanna Witecka; Anna Szydło; Ewa Gutmajster; Małgorzata Lisik; Aleksandra Auguściak-Duma; Maciej Tarnowski; Tomasz Czekaj; Hanna Czekaj; Aleksander L Sieroń
Journal:  Eur J Hum Genet       Date:  2008-10-01       Impact factor: 4.246

2.  Re: Consanguinity and isolated atrial septal defect in the North East of Iran.

Authors:  Mahmood Dhahir Al-Mendalawi
Journal:  Ann Saudi Med       Date:  2014 May-Jun       Impact factor: 1.526

  2 in total

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