일차성 Fanconi 증후군 1례

A Case of Primary Fanconi Syndrome

  • 강현호 (경희대학교 의과대학 소아과학교실) ;
  • 차성호 (경희대학교 의과대학 소아과학교실) ;
  • 조병수 (경희대학교 의과대학 소아과학교실)
  • Kang Hyeon-Ho (Department of Pediatrics, Kyunghee University, College of Medicine) ;
  • Cha Seong-Ho (Department of Pediatrics, Kyunghee University, College of Medicine) ;
  • Cho Byung-Soo (Department of Pediatrics, Kyunghee University, College of Medicine)
  • 발행 : 1998.05.01

초록

Fanconi syndrome is a renal disorder characterized by a generalized dysfuntion of the proximal tubule leading to excessive urinary losses of amino acids, glucose, phosphate, and bicarbonate. It is often associated with hypokalemia, hypophosphatemia, rickets, and osteomalacia. We have experienced one case of primary Fanconi syndrome. The patient was a 10 year old boy and his chief complaints were short stature, glycosuria, and genu valgum. There were aminoaciduria, hypokalemia, glycosuria, decreased TRP, and hypophosphaturia. We report a case of primary Fanconi syndrome with brief review of the literature.

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