scholarly journals Case Report: Direct Access Genetic Testing and A False-Positive Result For Long QT Syndrome

2015 ◽  
Vol 25 (1) ◽  
pp. 25-31 ◽  
Author(s):  
Sarah Predham ◽  
Sara Hamilton ◽  
Alison M. Elliott ◽  
William T. Gibson
Keyword(s):  
Case Report ◽  
Genetic Testing ◽  
Positive Result ◽  
Long Qt Syndrome ◽  
False Positive ◽  
Direct Access ◽  
False Positive Result ◽  
Long Qt ◽  
Qt Syndrome

Effect of clinical phenotype on yield of long QT syndrome genetic testing

Heart Rhythm ◽  
2005 ◽  
Vol 2 (5) ◽  
pp. S46 ◽  
Author(s):  
David J. Tester ◽  
Melissa L. Will ◽  
Carla M. Haglund ◽  
Michael J. Ackerman
Keyword(s):  
Genetic Testing ◽  
Long Qt Syndrome ◽  
Clinical Phenotype ◽  
Long Qt ◽  
Qt Syndrome

Endocrinopathies mimicking gene negative long QT syndrome

2021 ◽  
pp. 1-3
Author(s):  
Praloy Chakraborty ◽  
Jason D. Roberts ◽  
Michael H. Gollob
Keyword(s):  
Genetic Testing ◽  
Long Qt Syndrome ◽  
Qt Prolongation ◽  
Long Qt ◽  
Ventricular Repolarisation ◽  
Qt Syndrome ◽  
Hormonal Milieu

Abstract Ventricular repolarisation can be influenced by hormonal milieu which may mimic long QT syndrome. We describe a series of patients referred for genetic testing for diagnosed long QT syndrome where a detailed clinical workup demonstrated endocrinopathies as the cause of presumed “gene negative” long QT syndrome and QT prolongation.

scholarly journals Genetic testing for long QT syndrome and the category of cardiac ion channelopathies

PLoS Currents ◽  
2012 ◽  
Vol 4 ◽  
pp. e4f9995f69e6c7 ◽  
Author(s):  
Stephen M. Modell ◽  
David J. Bradley ◽  
Michael H. Lehmann
Keyword(s):  
Genetic Testing ◽  
Long Qt Syndrome ◽  
Long Qt ◽  
Qt Syndrome

scholarly journals Primary Carnitine Deficiency Presents Atypically with Long QT Syndrome: A Case Report

2011 ◽  
pp. 87-90 ◽  
Author(s):  
Irene De Biase ◽  
Neena Lorenzana Champaigne ◽  
Richard Schroer ◽  
Laura Malinda Pollard ◽  
Nicola Longo ◽  
...  
Keyword(s):  
Case Report ◽  
Long Qt Syndrome ◽  
Carnitine Deficiency ◽  
Long Qt ◽  
Qt Syndrome ◽  
Primary Carnitine Deficiency

Positron Emission Tomography: False Positive Result Due to Splenic Uptake in an Extension Study in Bronchial Carcinoma. A Case Report

2007 ◽  
Vol 93 (3) ◽  
pp. 316-318
Author(s):  
David Orts Giménez ◽  
Rosa Jiménez Yáñez ◽  
Gaspar Esquerdo Galiana ◽  
Antonia Galán Dávila ◽  
Eleuterio Llorca Martínez ◽  
...  
Keyword(s):  
Positron Emission Tomography ◽  
Case Report ◽  
Positive Result ◽  
False Positive ◽  
Bronchial Carcinoma ◽  
Emission Tomography ◽  
Extension Study ◽  
False Positive Result ◽  
Positron Emission ◽  
Splenic Uptake

Manifestation of Long QT syndrome with normal QTc interval under anesthesia: a case report

2011 ◽  
Vol 21 (12) ◽  
pp. 1265-1267 ◽  
Author(s):  
Banashree Mandal ◽  
Gurpreet Kaur ◽  
Yatindra K. Batra ◽  
Sachin Mahajan
Keyword(s):  
Case Report ◽  
Long Qt Syndrome ◽  
Qtc Interval ◽  
Long Qt ◽  
Qt Syndrome

scholarly journals Cost-Effectiveness of Genetic Testing in Family Members of Patients With Long-QT Syndrome

2011 ◽  
Vol 4 (1) ◽  
pp. 76-84 ◽  
Author(s):  
Marco V. Perez ◽  
Narmadan A. Kumarasamy ◽  
Douglas K. Owens ◽  
Paul J. Wang ◽  
Mark A. Hlatky
Keyword(s):  
Genetic Testing ◽  
Cost Effectiveness ◽  
Long Qt Syndrome ◽  
Family Members ◽  
Long Qt ◽  
Qt Syndrome

Prenatal diagnosis and treatment of fetal long QT syndrome: a case report

2002 ◽  
Vol 22 (13) ◽  
pp. 1209-1212 ◽  
Author(s):  
Ing-Kuang Chang ◽  
Ming-Kwang Shyu ◽  
Chien-Nan Lee ◽  
Miau-Ling Kau ◽  
Yu-Hsueh Ko ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Long Qt Syndrome ◽  
Diagnosis And Treatment ◽  
Long Qt ◽  
Qt Syndrome

scholarly journals Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing

Circulation ◽  
2018 ◽  
Vol 137 (6) ◽  
pp. 619-630 ◽  
Author(s):  
John R. Giudicessi ◽  
Dan M. Roden ◽  
Arthur A.M. Wilde ◽  
Michael J. Ackerman
Keyword(s):  
Genetic Variation ◽  
Genetic Testing ◽  
Long Qt Syndrome ◽  
Common Genetic Variation ◽  
Long Qt ◽  
Qt Syndrome

A novel variant of RyR2 gene in a family misdiagnosed as congenital long QT syndrome: The importance of genetic testing

2020 ◽  
Vol 60 ◽  
pp. 8-11
Author(s):  
Konstantinos P. Letsas ◽  
Efstathia Prappa ◽  
George Bazoukis ◽  
Louiza Lioni ◽  
Malena P. Pantou ◽  
...  
Keyword(s):  
Genetic Testing ◽  
Long Qt Syndrome ◽  
Long Qt ◽  
Novel Variant ◽  
Qt Syndrome ◽  
Congenital Long Qt Syndrome
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