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Unveiling primary Hyperoxaluria type 1: a fortuitous discovery through bone marrow biopsy

Taha Yassine Aaboudech1,2, Kaoutar Znati1,2, Ahmed Jahid1,2

  • 1Pathology Department, Ibn Sina Hospital, Rabat, Morocco.

Oxford Medical Case Reports
|October 28, 2024
PubMed
Summary

This case study reveals a rare instance of primary hyperoxaluria type 1 (PH1) diagnosed via bone marrow biopsy. Early detection of PH1 in children is crucial to prevent kidney damage and systemic oxalosis.

Keywords:
bone marrow biopsyhaematologyhistopathologyoxalate crystalsprimary hyperoxaluria

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