Clinical characteristics and mutation analysis of the RyR2 gene in seven Czech families with catecholaminergic polymorphic ventricular tachycardia

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F12%3A%230001622" target="_blank" >RIV/65269705:_____/12:#0001622 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1111/j.1540-8159.2012.03399.x" target="_blank" >http://dx.doi.org/10.1111/j.1540-8159.2012.03399.x</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1111/j.1540-8159.2012.03399.x" target="_blank" >10.1111/j.1540-8159.2012.03399.x</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Clinical characteristics and mutation analysis of the RyR2 gene in seven Czech families with catecholaminergic polymorphic ventricular tachycardia

Popis výsledku v původním jazyce

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare hereditary arrhythmia. The onset of clinical symptoms usually occurs during childhood, and is typically related to exercise. The aim of our study was to describe the clinical characteristics of seven Czech families with CPVT and the results of mutational analysis of the RyR2 gene in these families. Methods: The subjects and their relatives were investigated at the participating departments. They underwent basic clinical investigation, and history was focused on possible CPVT symptoms, i.e. syncopes during exercise. Bicycle ergometry was performed to obtain ECG recording during adrenergic stimulation. In all the investigated individuals blood samples were taken for mutation analysis of the RyR2 gene. Results: To date, seven families have been investigated, comprising 11 adults and 13 children. In seven CPVT patients the indication for examination was syncope during exercise. Diagnosis was confirmed by bic

Název v anglickém jazyce

Clinical characteristics and mutation analysis of the RyR2 gene in seven Czech families with catecholaminergic polymorphic ventricular tachycardia

Popis výsledku anglicky

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare hereditary arrhythmia. The onset of clinical symptoms usually occurs during childhood, and is typically related to exercise. The aim of our study was to describe the clinical characteristics of seven Czech families with CPVT and the results of mutational analysis of the RyR2 gene in these families. Methods: The subjects and their relatives were investigated at the participating departments. They underwent basic clinical investigation, and history was focused on possible CPVT symptoms, i.e. syncopes during exercise. Bicycle ergometry was performed to obtain ECG recording during adrenergic stimulation. In all the investigated individuals blood samples were taken for mutation analysis of the RyR2 gene. Results: To date, seven families have been investigated, comprising 11 adults and 13 children. In seven CPVT patients the indication for examination was syncope during exercise. Diagnosis was confirmed by bic

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FA - Kardiovaskulární nemoci včetně kardiochirurgie

OECD FORD obor

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Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2012

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Pacing and Clinical Electrophysiology

ISSN

0147-8389

e-ISSN

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Svazek periodika

35

Číslo periodika v rámci svazku

7

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

5

Strana od-do

798-803

Kód UT WoS článku

000305897500018

EID výsledku v databázi Scopus

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