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Coincidence of Andersen-Tawil syndrome and Marfan syndrome: A case report.

Authors :
Krych M
Ponińska J
Bilińska ZT
Płoski R
Biernacka EK
Source :
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc [Ann Noninvasive Electrocardiol] 2019 May; Vol. 24 (3), pp. e12624. Date of Electronic Publication: 2019 Jan 23.
Publication Year :
2019

Abstract

We report on a 44-year-old woman with coincidence of two genetic disorders: Andersen-Tawil syndrome and Marfan syndrome. In both, life-threatening arrhythmias could occur. A 44-year-old woman presented acute ascending aortic dissection with aortic arch involvement and chronic thoracic descending and abdominal aortic dissection. Clinical and genetic examination confirmed Marfan syndrome (MFS) diagnosis. Due to repolarization disorder in ECG and premature ventricular contractions in Holter ECG, the sequencing data were analyzed again and mutation in KCNJ2 gene was identified. The case showed that coincidence of Andersen-Tawil syndrome (ATS) and MFS did not provoke life-threatening arrhythmias. Complication was rather caused by expression of FBN1 mutation.<br /> (© 2019 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1542-474X
Volume :
24
Issue :
3
Database :
MEDLINE
Journal :
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc
Publication Type :
Academic Journal
Accession number :
30672637
Full Text :
https://doi.org/10.1111/anec.12624