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A Case of Fanconi Syndrome

Journal of the Korean Pediatric Society 1993;36(5):737-442.
Published online May 15, 1993.
A Case of Fanconi Syndrome
Young Woon Lee, In Seok Lim, Chul Ha Kim
Department of Pediatrics, College of Medicine, Chung Ang University, Seoul, Korea
Fanconi 증후군 1례
이용운, 임인석, 김철하
중앙대학교 의과대학 소아과학교실
Abstract
Fanconi syndrome is a complex of renal tubular dysfunction defined by glycosuria without diabetes, generalized aminoaciduria, phosphaturia, bicarbonaturia, uric aciduria, and renal tubular acidosis. It is often associated with hypokalemia, hypophosphatemia, rickets and osteomalacia. We have experienced one case of Fanconi syndrome with chronic tubulointerstitial nephritis. The patient was a 4 year and boy and his chief complaints were polyruia, polydipsia, and poor weight again. There were hyperchloremic metabolic acidosis, hypokalemia, glycosuria, generalized aminoaciduria and phosphaturia. We report a case of Fanconi syndrome with brief review of the literature.
Key Words: Fanconi syndrome


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