A case of Fanconi syndrome
Journal of the Korean Pediatric Society
;
: 737-742, 1993.
Article
in Korean
| WPRIM
| ID: wpr-89684
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 old and his chief complaints were polyuria, polydipsia, and poor weight gain. There were hyperchloremic metabolic acidosis, hypokalemia, glycosuria, generalized aminoaciduria and phosphaturia. We report a case of Fanconi syndrome with brief review of the literatures.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Osteomalacia
/
Polyuria
/
Rickets
/
Acidosis
/
Acidosis, Renal Tubular
/
Weight Gain
/
Hypophosphatemia
/
Fanconi Syndrome
/
Polydipsia
/
Glycosuria
Limits:
Child, preschool
/
Humans
Language:
Korean
Journal:
Journal of the Korean Pediatric Society
Year:
1993
Type:
Article
Similar
MEDLINE
...
LILACS
LIS