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Familial neurocardiogenic (vasovagal) syncope.

Authors :
Newton JL
Kerr S
Pairman J
McLaren A
Norton M
Kenny RA
Morris CM
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2005 Mar 01; Vol. 133A (2), pp. 176-9.
Publication Year :
2005

Abstract

Vasovagal syncope (VSS) is an exaggerated tendency towards the common faint caused by a sudden and profound hypotension with or without bradycardia. The etiology of VVS is unknown though several lines of evidence indicate central and peripheral abnormalities of sympathetic function. Studies however indicate a strong heritable component to the etiology of VVS in over 20% of cases. Here, we report the findings from a family that shows apparently autosomal dominant VVS in at least three generations. Clinical findings included an absence of any discernible cardiac or autonomic abnormalities and reproducible hypotension on tilt table testing in affected family members.<br /> ((c) 2005 Wiley-Liss, Inc.)

Details

Language :
English
ISSN :
1552-4825
Volume :
133A
Issue :
2
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
15666305
Full Text :
https://doi.org/10.1002/ajmg.a.30572