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Quest Diagnostics Launches Genetic Test to Assess Risk for Sickle Cell Anemia, Other Inherited Disorders
Couples who wish to know the risk of passing on a genetic disease such as sickle cell anemia to their children may now do so with QHerit, a new screening test by Quest Diagnostics.
The QHerit Pan-Ethnic Expanded Carrier Screen test covers 22 genetic diseases and was produced based on screening guidelines issued in March 2017 by the American College of Gynecology (ACOG). The test determines the likelihood of a couple passing on a heritable disorder to their children and its impact.
The test is able to predict the occurrence of diseases such as sickle cell anemia, cystic fibrosis, thalassemia, Joubert Syndrome 2, Tay-Sachs disease, and Fragile X syndrome, among others.
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This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.