1. Renal Tubular Dysfunction in a Patient with Beta-Thalassemia Minor
- Author
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Oktenli, C. and Bulucu, F.
- Abstract
Abstract β-Thalassemia minor is a hemoglobinopathy which has been known as a symptomless carrier state. Although there are many causes leading to renal tubular dysfunction, β-thalassemia minor has not been reported among them in reviewing the literature. In a 20-year-old male patient referred to us because of glucosuria detected with dipstick, there was also anemia (hemoglobin, 11.5 g/dl; mean cell volume, 60 fl; and mean cell hemoglobin concentration, 19.5 pg). The 24-hour urinary glucose excretion rate was 5 g and, additionally, he had tubular proteinuria (albumin/β2 -microglobulin ratio in urine was 17.32). Based upon the detailed evaluation for both asymptomatic urinary abnormality and anemia, he was diagnosed as having renal tubular dysfunction and β-thalassemia minor (hemoglobin A1 was 91%, and hemoglobin A2 was 9%). In conclusion, further reports are needed to reveal whether there is an association between these two distinct disorders.Copyright © 2002 S. Karger AG, Basel- Published
- 2002