Literature DB >> 15258623

Progressive familial heart block type II (PFHBII): a clinical profile from 1977 to 2003.

P Fernandez1, V A Corfield, P A Brink.   

Abstract

An evaluation of a 38-year-old Caucasian woman, who was referred to Tygerberg Hospital (Western Cape Province, RSA) with Wenckebach second-degree or possibly complete atrioventricular (AV) block that had progressed from first-degree AV block, identified a family history of the cardiac conduction system disorder progressive familial heart block type II (PFHBII). This prompted a retrospective clinical review of the subjects described in the original study, as well as additional family members who had not been examined in the original study. Progression of clinical features was observed, but more importantly, PFHBII was clinically redefined as an AV nodal disorder, which may progress to dilated cardiomyopathy (DCM).

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Year:  2004        PMID: 15258623

Source DB:  PubMed          Journal:  Cardiovasc J S Afr


  3 in total

1.  A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.

Authors:  Pedro Fernandez; Johanna Moolman-Smook; Paul Brink; Valerie Corfield
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

2.  A sluggish atrioventricular node.

Authors:  Tarun W Dasari; George Madden; Ralph Lazzara
Journal:  Indian Pacing Electrophysiol J       Date:  2010-06-05

Review 3.  Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch.

Authors:  P A Brink; J C Moolman-Smook; V A Corfield
Journal:  Cardiovasc J Afr       Date:  2009 Jan-Feb       Impact factor: 1.167

  3 in total

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