Real Cases of Rare Diseases - Primary Hyperoxaluria Type 1 (PH1)

CME: 1.0

September 30, 2021
/ Print / Reprints /
| Share More
/ Text Size+

Target Audience

This activity is designed to meet the educational needs of physicians, registered nurses and other healthcare professionals who specialize or have an interest in rare diseases, nephrology, urology, genetics and PH1.

Program Overview

This interactive case-based activity requires clinicians to make real-world decisions as they optimize diagnostic and therapeutic strategies for patients with suspected Alzheimer’s disease.

Throughout the activity practitioners will have the opportunity to immediately implement expert guidance and evaluate performance while addressing challenging questions about the latest clinical data and evidence-based recommendations.

Topics addressed include:

  • Differential diagnosis, including criteria and tools
  • Available and evolving therapeutic options
  • Tailoring treatment plans
  • Identifying and addressing obstacles to diagnosis and management

Learning Objectives

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

  • Review key clinical characteristics of PH1 and recommend strategies for its early and accurate diagnosis
  • Evaluate and integrate the latest clinical evidence for available and investigational treatments when tailoring treatment plans for patients with PH1
  • Summarize challenges related to the diagnosis and management of PH1 and implement strategies to address those challenges

Post a comment to this article