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Hematology/Oncology

Acute Intermittent Porphyria

An autosomal dominant metabolic disorder characterized by a 50% defect in activity of uroporphyrinogen I synthase.
CME credit is no longer available for this conference.

Course Authors

Robert G. Lerner, M.D.

In the past three years, Dr. Lerner has served as a consultant for RPR, and has served on the Speakers' Bureau for Pharmacia & Upjohn.

Release Date: 09/28/2002

 
Learning Objectives

Upon completion of this Cyberounds®, you should be able to:

  • Describe the clinical manifestations of acute intermittent porphyria

  • List the available therapy

  • Find a support group for AIP patients.

 

TERMS AND CONDITIONS

This conference may include discussion of commercial products and services.

The opinions expressed herein are those of the authors and do not necessarily represent the views of the sponsor or its publisher. Please review complete prescribing information of specific drugs or combination of drugs, including indications, contraindications, warnings and adverse effects before administering pharmacologic therapy to patients.

 

Please click below to accept the terms.

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