- A Case of Isolated Glycosuria Mediated by an SLC5A2 Gene Mutation and Characterized by Postprandial Heavy Glycosuria Without Salt Wasting
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Kim KM, Kwon SK, Kim HY
- KMID: 2369610
- Electrolyte Blood Press.
- 2016 Dec;14(2):35-37.
- doi: 10.5049/EBP.2016.14.2.35
Familial renal glycosuria (FRG) is an inherited disorder characterized by persistent glycosuria in the absence of hyperglycemia. It is caused by mutations in the sodium-glucose co-transporter, leading to increase in... -
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- A Case of Adult Fanconi's Syndrome with Glomerular Podocyte Foot Process Effacement and osteomalacia Induced by k Light Chain Disease
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Nam JH, Choi GH, Park KH, Ahn CW, Song YD, Lim SK, Lee HC, Huh KB
- KMID: 2199746
- J Korean Soc Endocrinol.
- 2000 Oct;15(4-5):627-633.
The Fanconi's syndrome is characterized by generalized disturbance of proximal tubular function. It leads to excessive losses of amino acids, glucose, phosphate, bicarbonate, and other substrates handled by the proximal... -
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- A Case of Tubulointerstitial Nephritis and Uveitis with Fanconi Syndrome
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Kim M, Kim HW, Kim JY, Jeong J, Park EJ, Kim J, Kim SM
- KMID: 2269087
- Korean J Med.
- 2015 Jun;88(6):711-714.
- doi: 10.3904/kjm.2015.88.6.711
Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disease that comprises 4.7% of acute interstitial nephritis. With reno-ocular manifestations, TINU syndrome is accompanied by symptoms such as fever, fatigue,... -
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- A case of adult Fanconi syndrome related with cadmium intoxi Seoul Korea
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No Authors Listed
- KMID: 2080813
- Korean J Med.
- 2001 Sep;61(3):276-280.
Adult Fanconi syndrome is a very rare disease characterized by renal glycosuria, generalized aminoaciduria, hypophosphatemia, hypouricemia and proximal renal tubular acidosis. It is divided into inherited and acquired forms. Proximal... -
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- Adult Idiopathic Renal Fanconi Syndrome: A Case Report
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Park DJ, Jang KS, Kim GH
- KMID: 2439087
- Electrolyte Blood Press.
- 2018 Dec;16(2):19-22.
- doi: 10.5049/EBP.2018.16.2.19
Renal Fanconi syndrome (RFS) is caused by generalized proximal tubular dysfunction and can be divided into hereditary and acquired form. Adult-onset RFS is usually associated with drug toxicity or systemic... -
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- Novel SLC5A2 Mutations and Genetic Characterization in Korean Patients with Familial Renal Glucosuria
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Lee WK, Oh SH, Chung WY
- KMID: 2435367
- Child Kidney Dis.
- 2018 Oct;22(2):37-41.
- doi: 10.3339/jkspn.2018.22.2.37
PURPOSE: Familial renal glucosuria (FRG, OMIM #233100) is a rare but relatively benign genetic condition characterized by persistent isolated glucosuria with a normal blood glucose level. We report three additional... -
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