Literature DB >> 484260

The Q-T syndrome--a family description.

P Andersson, L Lundkvist.   

Abstract

This paper describes a family of nine siblings of whom five suffer from the surdocardiac syndrome. All five are deaf-mute and have medical histories typical of the syndrome, with frequent syncopal attacks during the childhood, often caused by stress. Two of these five siblings have not suffered more than single attacks since puberty and are still alive. The other three had had continuous frequent attacks into adult years and died in connection with syncopes at 20, 27 and 37 years of age. The diagnosis, pathogenesis, treatment and genetics of the syndrome are discussed.

Entities:  

Mesh:

Year:  1979        PMID: 484260     DOI: 10.1111/j.0954-6820.1979.tb13472.x

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN: 0001-6101


  1 in total

1.  Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.

Authors:  Annika Winbo; Eva-Lena Stattin; Charlotte Nordin; Ulla-Britt Diamant; Johan Persson; Steen M Jensen; Annika Rydberg
Journal:  BMC Cardiovasc Disord       Date:  2014-02-19       Impact factor: 2.298

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.