Incomplete renal tubular acidosis in sickle cell disease
β Scribed by J.P. Goossens; L.W.Statius Van Eps; H. Schouten; A.L. Giterson
- Book ID
- 115819679
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- English
- Weight
- 709 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0009-8981
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π SIMILAR VOLUMES
Polyuria, hyposthenuria, hypomagnesemia, hypercalciuria, advanced nephrocalcinosis, low citrate excretion and low glomerular filtration rates were observed in two female siblings who were followed over 10 years. Acid loading revealed incomplete distal tubular acidosis. Hypomagnesemia was due to rena
Sickle cell anemia and the related hemoglobinopathies are associated with a large spectrum of renal abnormalities. The patients have impaired urinary concentrating ability, defects in urinary acidification and potassium excretion, and supranormal proximal tubular function. The latter is manifest by