NEW YORK - As a result of the Human Genome Project, we are now able to locate genetic mutations and know much more about a person's medical future than ever before. For genetic diseases that are endemic among certain peoples, such as the Icelandic, Ashkenazi Jewish, Old World Amish, and Micronesian populations, genetic testing programs designed to identify disease-related genes may prevent and treat diseases such as sickle-cell anemia, Tay Sach's disease, hemophilia, cystic fibrosis and others. What are some of the ethical issues being raised by the successful use of molecular genetic techniques and genetic screening of populations?

To examine advances in genomic medicine as well as ethical concerns, the New York Academy of Sciences' Genomic Medicine Discussion Group Section is sponsoring a meeting, Genetic Studies in Special Populations, on Wednesday, December 8 at Rockefeller University, Welch Hall in the Founder's Hall Building. Welch Hall can be reached through the E. 66th Street campus entrance. The meeting will run from 4 p.m. to 7 p.m.

The program features presentations by five top-notch researchers:

Harry Ostrer, Director of the Human Genetics Program at NYU Medical School

Topic: "A Genetic Profile of Jewish Peoples."

Genetic studies over the past half century have shed light on Jewish origins, the relatedness of Jewish communities, and the genetic basis of Mendelian disorders among Jewish peoples. Dr. Ostrer will discuss how these observations have been used to develop genetic testing programs and identify penetrance modifiers.

Erik Puffenberger, Clinic for Special Children Topic: "Molecular Genetics in Clinical Practice: Strategies for Disease Gene Identification, Characterization of Molecular Lesions, and Delivery of Efficient Diagnostic Testing in an Isolated Population."

Dr. Puffenberg will discuss his work at the Clinic for Special Children, a non-profit pediatric diagnostic a
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Contact: Jennifer Tang
jtang@nyas.org
212-838-0230 x257
New York Academy of Sciences
6-Dec-2004


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