SADS Focus on Timothy Syndrome
Although Timothy Syndrome is a rare disease, a number of new families affected by Timothy Syndrome contacted the SADS Foundation this year. An awareness campaign designed for anesthesiologists, pediatricians, cardiologists and neurologists is underway. Anesthesia is a known trigger of arrhythmias in Timothy Sydrome, therefore if surgical intervention is required for cardiac repair, extreme care in anesthesia selection and cardiac monitoring is essential to survival.
Salt Lake City, UT, May 11, 2012 --(PR.com)-- SADS Foundation to Focus on Timothy Syndrome
The Sudden Arrhythmia Death Syndromes (SADS) Foundation is leading the way when it comes to Timothy Syndrome research and outreach.
Although Timothy Syndrome is a rare disease, a number of new families affected by Timothy Syndrome contacted the SADS Foundation this year. An awareness campaign designed for anesthesiologists, pediatricians, cardiologists and neurologists is underway. Anesthesia is a known trigger of arrhythmias in Timothy Sydrome, therefore if surgical intervention is required for cardiac repair, extreme care in anesthesia selection and cardiac monitoring is essential to survival.
What is Timothy Syndrome?
Timothy Syndrome (TS) is a rare and serious genetic disorder characterized by a spectrum of complicated health concerns which include:
- abnormally prolonged QT predisposing a child to serious cardiac events including cardiac arrest and sudden death,
- syndactyly (webbing between or apparent fusing) of fingers or toes
- congenital heart defects (structural heart anomalies present at birth),
- facial anomalies,
- weakened immune system,
- developmental delays and autism.
“It is only through continued identification and research of the families affected by Timothy Syndrome that we can change the ultimate outcome for these children,” said Katherine Timothy for whom the Syndrome is named.
About The SADS Foundation
Formed in 1992, the SADS (Sudden Arrhythmia Death Syndromes) Foundation’s mission is to save the lives and support the families of children & young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. We are committed to promoting the early detection and treatment of these conditions throughout the world. The Foundation distributes materials internationally through grass roots efforts in order to teach families, educators and medical professionals about SADS conditions.
SADS (Sudden Arrhythmia Death Syndromes) Foundation
Phone: 1.800.STOP-SAD (800.786.7723) www.StopSADS.org
Facebook: www.causes.com/causes/225843
Twitter: www.twitter.com/SADSFoundation
Contact: Laura Wall
VP, Development & Marketing
Office: 801.531.0937
Cell: 801.641.7148
E-mail: laura@sads.org
The Sudden Arrhythmia Death Syndromes (SADS) Foundation is leading the way when it comes to Timothy Syndrome research and outreach.
Although Timothy Syndrome is a rare disease, a number of new families affected by Timothy Syndrome contacted the SADS Foundation this year. An awareness campaign designed for anesthesiologists, pediatricians, cardiologists and neurologists is underway. Anesthesia is a known trigger of arrhythmias in Timothy Sydrome, therefore if surgical intervention is required for cardiac repair, extreme care in anesthesia selection and cardiac monitoring is essential to survival.
What is Timothy Syndrome?
Timothy Syndrome (TS) is a rare and serious genetic disorder characterized by a spectrum of complicated health concerns which include:
- abnormally prolonged QT predisposing a child to serious cardiac events including cardiac arrest and sudden death,
- syndactyly (webbing between or apparent fusing) of fingers or toes
- congenital heart defects (structural heart anomalies present at birth),
- facial anomalies,
- weakened immune system,
- developmental delays and autism.
“It is only through continued identification and research of the families affected by Timothy Syndrome that we can change the ultimate outcome for these children,” said Katherine Timothy for whom the Syndrome is named.
About The SADS Foundation
Formed in 1992, the SADS (Sudden Arrhythmia Death Syndromes) Foundation’s mission is to save the lives and support the families of children & young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. We are committed to promoting the early detection and treatment of these conditions throughout the world. The Foundation distributes materials internationally through grass roots efforts in order to teach families, educators and medical professionals about SADS conditions.
SADS (Sudden Arrhythmia Death Syndromes) Foundation
Phone: 1.800.STOP-SAD (800.786.7723) www.StopSADS.org
Facebook: www.causes.com/causes/225843
Twitter: www.twitter.com/SADSFoundation
Contact: Laura Wall
VP, Development & Marketing
Office: 801.531.0937
Cell: 801.641.7148
E-mail: laura@sads.org
Contact
SADS Foundation
Laura Wall, Vice President
801-641-7148
www.StopSADS.org
Laura Wall, Vice President
801-641-7148
www.StopSADS.org
Contact
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