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Dr. Alison Jazwinski discusses how to appropriately diagnose hemochromatosis and understand the workup and management of the disease.

Educational objectives:

Upon completion of this activity, participants should be able to:

  • Discuss the percentage of patients with hereditary iron overload syndromes that will be homozygous for the C282Y mutation
  • Describe initial screening test to assess whether a patient has hereditary hemochromatosis
  • List causes of secondary iron overload

Reading Resources:

  1. Bacon. Hepatology 2011;54:328.
  2. Pietrangelo. Gastro 2010;139:393.
  3. Ludvigsson JF, Murray JA, Adams PC, Elmberg M. Scand J Gastroenterol. 2012 Dec 20.

Disclosures:

Dr. Jazwinski has no relevant relationships with any entities producing health care goods or services.

Accreditation Statement:

The University of Pittsburgh School of Medicine is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

The University of Pittsburgh School of Medicine designates this enduring material for a maximum of 0.50 AMA PRA Category 1 CreditsTM. Each physician should only claim credit commensurate with the extent of their participation in the activity. Other health care professionals are awarded (0.05) continuing education units (CEU) which are equivalent to 0.50 contact hour.

For your credit transcript, please access our website 4 weeks post-completion at http://ccehs.upmc.edu and follow the link to the Credit Transcript page. If you do not provide the last 5 digits of your SSN on the next page you will not be able to access a CME credit transcript. Providing your SSN is voluntary.

Release Date: 2/14/2013 | Last Modified On: 7/14/2014 | Expires: 7/14/2015

This course has been expired.