Publications by authors named "Mohamed BenHmida"
Curr Rheumatol Rev
June 2024
Article Synopsis
- Primary hyperoxaluria is a genetic disorder affecting the glyoxylate pathway, leading to poor oxalate breakdown and complications like kidney and joint diseases, with neonatal oxalosis being the most severe form.
- A 55-year-old male on hemodialysis for end-stage renal failure and diagnosed with primary hyperoxaluria presented with inflammatory joint issues and various calcifications, but his condition continued to worsen despite treatment.
- The case highlights that primary hyperoxaluria can have late-onset symptoms and long-term complications beyond kidney issues, contributing to a complex medical picture.
