hyperoxalurie hereditaire [oxalose] [a propos d'un cas]

ABSTRACT

We report one case primary hyperoxaluria in a fourteen year old child. The diagnosis was possible after the discovery of oxalate of Ca crystals in kidneys and marrow. Our case illustrates some of the clinical and paraclinical characteristics of oxalosis. It also proves how severe the kidney failure could be in this disease. The diagnosis criteria and the therapeutic possibilities that lead to improve this diseasee are also discussed here