A Case of the Fanconi Syndrome with Nephrocalcinosis.
- Author:
Young Mi KIM
1
;
Seong Shik PARK
;
Ju Suk LEE
;
Su Yung KIM
Author Information
1. Department of Pediatrics, College of Medicine, Pusan National University, Busan, Korea. suyung@pusan.ac.kr
- Publication Type:Case Report
- Keywords:
Fanconi syndrome;
Hypercalciuria;
Nephrocalcinosis
- MeSH:
Child;
Cholecalciferol;
Cleft Lip;
Dehydration;
Diagnosis, Differential;
Fanconi Syndrome*;
Gait;
Genu Valgum;
Glycosuria;
Humans;
Hypercalciuria;
Hypophosphatemia, Familial;
Kidney;
Korea;
Male;
Nephrocalcinosis*;
Palate;
Physical Examination;
Proteinuria;
Reference Values;
Rickets;
Ultrasonography
- From:Journal of the Korean Society of Pediatric Nephrology
2003;7(2):234-238
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Fanconi syndrome is a generalized functional disorder of the proximal tubule of the kidney and is characterized by aminoaciduria, glycosuria, hyperphosphaturia, dehydration, rickets, and growth failure. Nephrocalcinosis and hypercalciuria are rare manifestations of Fanconi syndrome. There is no case report of Fanconi syndrome complicated with nephrocalcinosis and hypercalciuria in Korea. A 6-year-old boy presented with genu valgum and waddling gaits for about 3 years. There was no family history of renal disease and his physical examination was normal except for genu valgum and corrected cleft lip and palate. Laboratory investigations showed generalized aminoaciduria, glycosuria, hyperphosphaturia, hypercalciuria, and low-molecular weight proteinuria including beta2-microglobulin. Serum 25-OH vitamin D3 was within the normal range, and 1,25-(OH)2 vitamin D3 was elevated. Bilateral renal medullary hyperechogenicity was demonstrated by ultrasonography. Analysis of the CLCN5 gene revealed no mutation. Here we describe a boy with Fanconi syndrome complicated with nephrocalcinosis and discuss the differential diagnosis.
