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Those List members advocating the registering of PWP might be
interested in noting that the Cleveland Clinic Center for Colon
Polyps and Colon Cancer has such a list of colon patients whose
relatives, because of inherited gene mutation, are at risk of
getting colorectal cancer.

In the Spring issue of the Cleveland Clinic _Vistas_ (vol 6 #1 pp
14-15) it says "Because their risk is so high, these patients
should be in a registry that provides scheduled screening
examinations for early detection of precancerous polyps and
cancer."

Quoting from the article, "The Cleveland Clinic Jagelman
Registries ... contain information on more than 700 families and
5,000 individuals who are at high risk for one of the five forms
of inherited colorectal cancer due to their family and personal
history.  Some patients in the registry have undergone genetic
testing to determine what specific mutations are present in the
DNA."

In its 20-year history, the Jagelman Registries have played an
important role in advancing the understanding of inherited colon
cancer by providing a wealth of information on high-risk
individuals and families.  Cleveland Clinic colorectal cancer
specialists recently have begun work on a National Cancer
Institute project to develop a larger, population-based colon
cancer registry.  The Clinic participates in a research
consortium that is one of six cancer study groups selected for
the project. "By comparing data from the known high-risk
population in the Jagelman Registries with that from other
centers, we hope to better understand the interaction between
environmental effects and inherited colon cancer risk."

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  Sid Roberts   68/dx3
  [log in to unmask]       Youngstown, Ohio