Uncontrolled diabetic with septicaemia: Plain films show left perinephric, renal parenchymal, and collecting systems gas and possible pararenal gas. IVP shows no function on left. Female
17 year Female, black just matriculated. Primary Hyperoxluria (in one place called ¡§hyperoxlarmia¡¨? mistakenly). Acute ureteric colic. July 2000. Renal calculi. (Lost brother aged 9 years chronic renal failure ¡V dialysed hyperoxyluria). Sent from Bloemfontein for assessment for renal and liver transplant (apparently accepted). On dialysis since August 2000 chronic renal failure. Renal biopsy marked nephrocarcinosis ¡V calcium oxalate crystals in tubules. Primary hyperoxyluria: Autosomal recessive. Type I Alteration in glyoxalate metabolism. Type II D-Glyceric dehydrogenase deficiency with types result in calcium oxalate deposition in various tissues including kidneys, muscles retina increased urinary oxalate in urine. Nephrolithiasis ?³ Nephrocalcinosis.
