TITLE:
Primary Hyperoxaluria Type 1 in Adulthood: Case Series
AUTHORS:
Sara El Maakoul, Nada El Kadiri, Nabil Hmaidouch, Salma Belmokadem, Loubna Benamar, Tarik Bouattar, Naima Ouzeddoun
KEYWORDS:
Primary Hyperoxaluria, Adulthood, Kidney Disease
JOURNAL NAME:
Open Journal of Nephrology,
Vol.14 No.3,
August
30,
2024
ABSTRACT: Introduction: Primary hyperoxaluria type 1 (HP1) is a rare lithiasis with systemic involvement, due to the accumulation of calcium oxalate crystals. In the absence of therapeutic management, it progresses to end-stage chronic renal failure. The aim of this study is to describe and analyse the observations of our patients with HP1. Patients and methods: This is a retrospective study carried out between 2014 and 2023 in the Nephrology-Dialysis Transplant Department of the Ibn Sina University Hospital in Rabat. The clinical, paraclinical and evolutionary elements were taken from the patients’ medical records. Results: We collected 11 cases, with a mean age of 27 ± 8.5 years and a M/F sex ratio of 1.7. The diagnosis of HP1 was made on the basis of genetic analysis in 8 patients, morphological and spectro-photometric analysis of the calculus in one patient, biopsy of the graft in one patient and crystalluria and a family history of PH1 in one patient. Two patients died, and 8 patients were on chronic haemdialysis with systemic damage. Only one patient maintained a stable GFR at 60 ml/min. Conclusion: Early diagnosis combined with conservative treatment is the only way to limit the rapid progression of this disease. This requires awareness and collaboration between nephrologists, urologists and biologists within a specialised team.