Latest Long QT syndrome Stories
In a first-of-its-kind study, researchers from the United States and Europe discovered genetic mutations associated with long QT syndrome (LQTS), a genetic abnormality in the heart's electrical system, in a small number of intrauterine fetal deaths.
In a molecular genetic evaluation involving 91 cases of intrauterine fetal death, mutations associated with susceptibility to long QT syndrome (LQTS; a heart disorder that increases the risk for an irregular heartbeat and other adverse events) were discovered in a small number of these cases, preliminary evidence that may provide insights into the mechanism of some intrauterine fetal deaths.
Some antidepressants known as SSRIs have been found to pose a small but serious risk on users’ hearts, according to new research.
Genetic researchers have made an important step towards resolving the mystery of the causes of intrauterine fetal demise (IUFD), or stillbirth, where a baby dies in the womb after the 14th week of gestation.
250,000 people in the U.S. die from sudden cardiac arrest every year. Now, a genetic variant in a cardiac protein could be linked to heart rhythm dysfunction.
What if reconstructing your family tree could possibly help save your life?
Reconstructing family trees dating back to 1811, Dutch researchers have estimated the death risk for people with inherited heart rhythm disorders.