References in periodicals archive ?
Detecting or confirming the subtype of LQTS through genetic testing can also play a role in guiding therapy through lifestyle modifications and drug treatment.
c] interval; nevertheless, it reduces TDP and can therefore be used safely for anesthesia induction and maintenance in children with LQTS (5).
Almost all (98%) consider LQTS and other genetic CCs in SUD.
Acquired LQTS is much more common than congenital LQTS.
17%) out of total 379, definitely have LQTS according to Schwartz criteria10.
Now, Brugada syndrome, like LQTS, is a pure ECG diagnosis.
Researchers from Columbia University Medical Center used iPSCs differentiated into cardiomyocytes (iPSCs-CMs) to study the physiological basis for arrhythmias in a four-year-old with LQTS.
All of the LQTS athletes seen during the period of study were managed via the same protocol, which, at the Mayo Clinic, includes providing the patients and their families with information to enable them to make decisions regarding continued sports participation.
Current guidelines disqualify most LQTS patients from almost every sport.
LQTS refers to a group of disorders defined by delayed cardiac repolarization as manifested by a prolonged QT interval on ECG.
It has proven to be very accurate in diagnosing LQTS.
There are many potential challenges to the reliable diagnosis of LQTS.
Acronyms browser ?
Full browser ?
- Lr dose
- LR Dragstedt
- LR Princeteau
- LR RDA
- LR Technologies