Myeloproliferative disorders occur in families, thus giving rise to the theory that it is a genetic disease that may be caused by an abnormal gene in the DNA that can be passed from one generation of family members to another. DNA can be gathered from family members through blood samples and the investigators will investigate (through DNA testing) to see if there are abnormal genes that may be responsible for causing the MPDs. Understanding which genes are responsible for causing MPDs can help develop ways to identify people who may be at risk for developing an MPD, allow for the development of better treatments, possibly a cure, or even prevent the development of MPDs.
Study Type
OBSERVATIONAL
Enrollment
17
Georgetown University
Washington D.C., District of Columbia, United States
University of Illinois at Chicago
Chicago, Illinois, United States
Mount Sinai School of Medicine
New York, New York, United States
Weill Cornell
New York, New York, United States
University of Utah
Salt Lake City, Utah, United States
University of Florence
Florence, Italy
To determine a linkage from the DNA analyzed to find a gene that will allow for genetic evaluation of families with MPDs.
Time frame: 3 years
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