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'Do It Yourself' Genetic Test Kit Promoted During 2005 Hemochromatosis Awareness Month
"Do it yourself!" is a suggestion
often made by Sandra Thomas, founder and president of the American
Hemochromatosis Society, a non-profit health
organization based near Orlando, Florida. Thomas, a nationally recognized
patient advocate, is referring to family genetic screening for hereditary
hemochromatosis (HH), also known as genetic iron poisoning or iron overload
disease, the most common genetic disease in the USA, according to the Centers
for Disease Control and Prevention (CDC). Genetic testing for the disease has
been commercially available through doctors' offices since 1997, but most
patients have never been tested for it. This is a tragic health situation,
which Thomas wants to change through "do-it-yourself" genetic test kits and
iron storage screening performed by patients themselves.
May 2005 is the American Hemochromatosis Society's annual "National
Hereditary Hemochromatosis Genetic Screening Month," and, Thomas, once again
is urging the public to use DAT (Direct Access Testing) to confirm, or rule
out HH, in their families. When Thomas discovered that HealthCheckUSA
(http://www.healthcheckusa.com ), a San Antonio, Texas-based
company, offered
direct testing, she immediately contacted Holt Vaughn, director, and urged him
to add the hemochromatosis DNA genetic test kit and the iron blood tests-
transferrin saturation percentage and serum ferritin to the menu of tests his
company offered to the public.
Patients with the hemochromatosis gene mutations absorb excess iron from a
normal diet. Symptoms, which can be devastating and costly to the health care
system, include: chronic fatigue, infertility, arthritis, diabetes, sudden
heart attack, primary liver cancer, and liver failure/heart failure resulting
in the need for a liver and/or heart transplant. Hemochromatosis is treated
through "bloodletting" identical to blood donation and is the treatment of
choice for the disease. Hemochromatosis can affect men, women and children.
In addition to an estimated 37 million "silent carriers" of HH, this country
has another 2 to 3 million Americans who are at high risk for having
hereditary hemochromatosis.
The American Hemochromatosis Society can provide doctors and patients with
interviews/photos. Contact information: Sandra Thomas, President, or David G.
Snyder, Vice President, American Hemochromatosis Society, 407-829-4488,
Email: mail@americanhs.org, Web site: http://www.americanhs.org . Additional
information about the DNA genetic self-test kit for hemochromatosis can be
obtained from Holt Vaughn, President of HealthCheckUSA, at:
http://www.healthcheckusa.com , Email: holt@healthcheckusa.com , Business:
1(800) 299-7226 x. 228 .
The American Hemochromatosis Society
http://americanhs.org
http://www.healthcheckusa.com
"Do It Yourself" Genetic Test Kit promovat Pe parcursul anului 2005 Hemochromatosis ConÂștientizarea Luna - 'Do It Yourself' Genetic Test Kit Promoted During 2005 Hemochromatosis Awareness Month - articole medicale engleza - startsanatate