long QT syndromemutationBACKGROUND: A proportion of patients with congenital long QT syndrome (LQTS) experience potentially life-threatening cardiac arrhythmias. AIM: To examine whether depressive symptoms are related to arrhythmic events among symptomatic and asymptomatic LQTS patients, and syncope events...
congenital heart diseases, including long QT syndrome sarcoidosis electrolyte imbalances Sinus tachycardia has some unique causes, including: exercise anxiety or fright severe emotional distress fever pain Bradycardia causes Some potential causes of bradycardia include: problems with the heart’s sinus node ...
The congenital long QT syndrome (LQTS) is an inherited disorder characterized by a delay in cardiac cellular repolarization leading to cardiac arrhythmias ... DW Wang,K Yazawa,N Makita,... - 《Journal of Clinical Investigation》 被引量: 349发表: 1997年 Improved safety and reduction in stent ...
symptoms may have important roles in determining general anxiety, depression and physical health in at-risk individuals of inherited cardiac disorders, the present findings may have implications for the further development of genetic counseling for this patient group. introduction long qt syndrome (...
Risk of QT prolongation:Due to an increased risk of prolonging the QT interval, Lucemyra should be avoided in patients with congenital long QT prolongation and electrocardiographs should be monitored in higher risk patients. Clinical Efficacy
A gain-of-function mutation in Cav1.2 causes Timothy syndrome (TS), an autosomal dominant developmental disorder [46]. This syndrome is a multiorgan disorder associated with malformations, cardiac symptoms (long QT), and neurological developmental defects [46,47,48], including manifestation of ...
Patient with Prinzmetal angina and syndrome X have an excellent prognosis with little risk of long term heart damage. Is it possible to prevent angina? The risk for atherosclerotic heart disease can be minimized by preventive medicine. Exercise, a healthy diet, and avoiding smokingwill decrease the...
Annals of MedicineHintsa, T., Keltikangas-Jarvinen, L., Puttonen, S., Ravaja, N., Toivonen, L., Kontula, K., & Swan, H. (2009). Depressive symptoms in the congenital long QT syndrome. Annals of Medicine, 23, 1-6.Hintsa, T., Keltikangas-Jarvinen, L., Puttonen, S., Ravaja,...
Type and reproducibility of symptoms in genotyped congenital long QT patientsangiotensin IInitric oxide synthase uncouplingnox expressioncGMP-dependent protein kinasevasodilator-stimulated phosphoproteinLipid-lowering agents have been shown to reduce morbidity and mortality associated with coronary artery disease (...
OBJECTIVES: Recently, two ion channels associated with congenital long QT syndrome, the SCN5A-encoded Nav1.5 sodium channel and the KCNH2-encoded HERG potassium channel (IKr), have been found on gastrointestinal smooth muscle and interstitial cells of Cajal. The aim of this study was to ...