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UPMC Cancer Centers, Working in Tandem with the University of Pittsburgh Cancer Institute, Pittsburgh Pennsylvania USA UPMC Cancer Centers, Working in Tandem with the University of Pittsburgh Cancer Institute, Pittsburgh Pennsylvania USA

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Genetic Counseling Services

Overview

Genetic Counseling Services at UPMC Cancer Centers is coordinated through the Cancer Genetics Program (a joint program of UPMC, the University of Pittsburgh Cancer Institute and Magee-Womens Hospital) and provides education, research and cancer risk assessment for individuals and their families who are concerned about their risk for cancer and how genetic inheritance may play a role.

Genetic Counseling Services strives to provide expert clinical consultation in cancer genetics, develop a cohort of patients and families with hereditary cancer for a variety of research studies and provide training and continuing medical education to medical professionals.

This comprehensive program:

  • offers genetic counseling for determining cancer risk
  • provides opportunities to learn about cancer screening and genetic testing
  • presents medical geneticists and genetic counselors that are specially trained in cancer genetics and certified by the American Board of Medical Genetics
  • helps people and their families understand how certain cancers may cluster in families
  • educates people on the most current and available genetic testing
  • informs people about which cancer-screening tests may offer early detection
  • offers individualized prevention steps that make sense for each person.

Patients undergo genetic consultation and, in specific cases, pursue targeted genetic testing for hereditary cancer syndromes such as:

  • Hereditary Breast-Ovarian Cancer (BRCA1, BRCA2)
  • Li-Fraumeni Syndrome (TP53)
  • Cowden Syndrome (PTEN)
  • Von Hippel-Lindau Disease (VHL)
  • Familial Adenomatous Polyposis (APC)
  • Hereditary Non-polyposis Colorectal Cancer (MSH2, MLH1)
  • Multiple Endocrine Neoplasia Type 1 (MEN1)
  • Multiple Endocrine Neoplasia Type 2 (RET)
  • Hereditary Paraganglioma (SDHD)
  • Familial Melanoma (CDKN2A)
  • Nevoid Basal Cell Carcinoma Syndrome (PTCH).

Cancer risk consultation can relieve anxiety and provide a sense of control. After a complete review of your family and medical history, the consultation team will discuss the following information:

  • an estimation of your risks for specific cancers based upon your age, family history and other risk factors
  • a complete analysis of your family tree
  • the possible role of genetics in your family's cancer; emotional issues surrounding cancer and risk
  • the availability of genetic testing for certain cancers and the risks, benefits and limitations of genetic testing
  • cancer screening tests and recommendations for how often you should be screened.

More information:

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For more information about any of the services available at UPMC Cancer Centers, please call the UPMC Cancer Centers Information and Referral Service at 412-647-2811 or send us an e-mail via "Ask a Question Online."

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