Primary hyperoxaluria type I is a rare autosomal show reflux. Cystoscopy with retrograde urogram showed no evidence of obstruction. A diagnosis of recessive metabolic disorder characterized by absence of liver specific peroxisomal alanine glyoxylate aminoend-stage renal disease (ESRD) of unknown aetiology was made. Live related donor kidney transplant was transferase (AGT ) leading to elevated ...

Key words: combined liver/kidney transplantation; reference range of 20–40 mmol/l. Prior to analysis, an nephrocalcinosis; primary hyperoxaluria ultrafiltration of plasma to remove proteins and others molecules was performed. Urine ion chromatography was used for measuring urine oxalate concentration with a reference range of

Primary hyperoxaluria (PH) has heterogeneous renal manifestations in infants and children. This often leads to delay in diagnosis. In the past 3 years, genetic samples were sent for seven children with a clinical diagnosis of PH. Their medical records were reviewed for clinical presentation and outcomes. Of the seven children, three were males. The median age of presentation was 4.9 years with ...

A case is presented in which primary hyperoxaluria and oxalosis in a 14-year-old Caucasian female were diagnosed. Generalized root resorption resulted in a remarkable mobility of her maxillary central and lateral incisors, although no bone loss was noted. The management of the patient's dental concerns in this rare heritable metabolic disorder consisted of removing the maxillary incisor teeth a...

Nephrolithiasis remains a major health problem in Western countries. Seventy to 80% of kidney stones are composed of calcium oxalate, and small changes in urinary oxalate affect risk of kidney stone formation. Intestinal oxalate secretion mediated by the anion exchanger SLC26A6 plays an essential role in preventing hyperoxaluria and calcium oxalate nephrolithiasis, indicating that understanding...

Oxalate nephropathy is a rare pathology that can be difficult to diagnose. It results from calcium oxalate crystals are deposited in the renal interstitium or tubules. Once deposition ensues, multitude of complications occur, including failure. One etiology for lack biliary acid. The diagnosis typically based on visualization tubules biopsy, and treatment range simple removal offending agent ch...

A perfusion technique has been used to study the effect of sodium chenodeoxycholate (5 mmol 1-1) on absorption of oxalate (2 mmol 1-1) from the surgically excluded colon in two patients with chronic liver disease. Colonic absorption of oxalate increased at least fivefold when sodium chenodeoxycholate was incorporated in the perfusion solutions. This observation may explain enteric hyperoxaluria...