Reach Me Foundation

Picture 1

Learn More about Funding for Scholarships and Recipients.

Recipients for 2011

Jerel Brown
Joel Brown
Chanel Fraser
Lorence Garrett
Darren Jenkins
Jump to navigation 1. 877. 274. 9432 search form search this site clinical research hipaa and licenses billing and insurance contact us about us order tests long qt syndrome (lqts) long qt syndrome (lqts) is an electrical heart disorder associated with a high risk for life-threatening arrhythmias. viagra without a doctor prescription buy cheap viagra buy cheap viagra viagra for sale cheap generic viagra buy cheap viagra viagra online cheap viagra online viagra without a doctor prescription generic viagra online It is a genetic disease resulting from mutations within genes that encode cardiac ion channels or proteins that modulate the function of cardiac ion channels, thus lqts is often referred to as a “cardiac channelopathy" (1). The value of lqts genetic testing has been documented extensively in the medical literature, and multiple medical societies have issued consensus statements and guidelines recommending genetic testing for all lqts patients to enable accurate risk stratification, guide therapeutic strategies and to identify potentially at-risk family members (2,3). 2011 hrs/era expert consensus recommendations on lqts genetic testing index patients with established or suspected clinical diagnosis family members recommended: for diagnosed/suspected patients or asymptomaticâ patients with idiopathic, serial qtc values >480ms (prepuberty) or >500 ms (adults) may be considered: for asymptomatic patients with idiopathic, serial qtc values >460ms (prepuberty) or > 480 ms (adults) recommended adapted from: ackerman mj, priori sg, willems s, berul c, et al. Hrs/ehra consensus statement on the state of genetic testing for channelopathies and cardiomyopathies. Heart rhythm. 2011;8:1308-39. Lqts is estimated to affect 1 in 2,500 individuals. 1 lqts may present as syncope, seizure and/or sudden cardiac death. These symptoms are often occur in response to a specific trigger such as exercise or emotional stress. While the symptoms associated with lqts commonly present during childhood and adolescence, the risk of initial and repeat cardiac events persists into adulthood (4,5). â  ecg results often reveal prolonged ventricular repolarization (qt-interval prolongation), although approximately one-third of lqts patients have a qt interval that overlaps those of normal, healthy individuals thereby rendering ecg analysis alone insufficient to diagnosis lqts (6). Lqts is typically inherited in an autosomal dominant pattern, in which a single mutation causes disease. All first-degree relatives (i. E. , siblings, parents and children) of an individual with an lqts gene mutation have up to a 50% risk of harboring the same mutation. Importantly, family members who have no apparent symptoms and a normal qt interval may still be at risk for cardiac events. Most silent carriers do not present with the typical lqts phenotype and therefore require genetic testing to confirm the presence or absence of disease (7). â  â . Nima Sheel
Courtney Short
Kristyl Smith

Tameka Spikes
Tara Spikes
Shaina C. Williams
Matthew Wilson

Learn more about the Recipients of the 2011 Reach Me Foundation Scholarship