Interactive Case: PH1

CE / CME

Diagnosis and Management of Primary Hyperoxaluria Type 1: An Interactive Case Challenge

Physician Assistants/Physician Associates: 1.00 AAPA Category 1 CME credit

Nurses: 1.00 Nursing contact hour

Physicians: maximum of 1.00 AMA PRA Category 1 Credit

Released: December 12, 2023

Expiration: December 11, 2024

David S. Goldfarb
David S. Goldfarb, MD, FASN, FNKF

Activity

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Which of the following is a symptom consistent with primary hyperoxaluria type 1 (PH1) in children that would require a nephrology assessment?

All of the following diagnostic tests are recommended for most patients suspected of having primary hyperoxaluria (PH) EXCEPT which one?

A 14-year-old with PH1 diagnosed by AGXT genetic mutation presents after being unresponsive to vitamin B6. This patient would like something easy for compliance, as he lives far from a medical community. Which of the following would you recommend as the optimal treatment option for this patient?