- 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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- Adefovir-induced Fanconi syndrome associated with osteomalacia
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Park S, Kim WI, Cho DH, Kim YJ, Kim HS, Kim JH, Cha SK, Park KS, Lee JH, Lee SM, Lee EY
- KMID: 2428762
- Clin Mol Hepatol.
- 2018 Sep;24(3):339-344.
- doi: 10.3350/cmh.2017.0009
Fanconi syndrome is a dysfunction of the proximal renal tubules that results in impaired reabsorption and increased urinary loss of phosphate and other solutes. The pathophysiology of drug-induced Fanconi syndrome... -
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- Three Cases of Osteomalacia with Fractures Induced by Adefovir in Chronic Hepatitis B
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Kim AR, Choi YJ, Chung YS
- KMID: 2155133
- Osteoporosis.
- 2015 Dec;13(2):109-116.
- doi: 10.0000/ost.2015.13.2.109
Adefovir dipivoxil is used antiviral agent in the treatment of chronic hepatitis B virus infection. This drug is recommended for patients infected with lamivudine-refractory hepatitis B. Many studies of low-dose... -
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- Ga68-DOTA Peptide PET/CT to Detect Occult Mesenchymal Tumor-Inducing Osteomalacia: A Case Series of Three Patients
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Ho CL
- KMID: 2052058
- Nucl Med Mol Imaging.
- 2015 Sep;49(3):231-236.
- doi: 10.1007/s13139-015-0328-2
Tumor-induced osteomalacia (TIO) is a rare disease that manifests with paraneoplasic syndrome and overproduction of fibroblast growth factor 23 (FGF23), leading to renal phosphate wasting and hyperphosphaturia, eventually leading to... -
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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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- Phosphaturia as a Promising Predictor of Recurrent Stone Formation in Patients with Urolithiasis
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Ha YS, Tchey DU, Kang HW, Kim YJ, Yun SJ, Lee SC, Kim WJ
- KMID: 2314710
- Korean J Urol.
- 2010 Jan;51(1):54-59.
PURPOSE: Recent studies have suggested that renal phosphate leakage and the associated phosphaturia are significant underlying causes of calcium urolithiasis. The aims of this study were to assess whether phosphaturia... -
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- A Case of Multiple Myeloma with Ameliorated Bone Pain after Treatment of Adult Fanconi Syndrome
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Kwon HL, Cho SJ, Song YS, Song HH, Oh JE, Kim SJ, Kim HJ, Noh JW
- KMID: 2253232
- Korean J Nephrol.
- 2008 Jul;27(4):481-486.
Adult Fanconi syndrome is characterized by variable abnormalities caused by renal proximal transport defects, resulting in glycosuria, aminoaciduria, bicarbonaturia, uricosuria and phosphaturia. A 57-year-old man with kappa-light chain multiple myeloma,... -
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- Two Cases of Oculocerebrorenal Syndrome in Two Brothers Diagnosed after Congenital Cataract Surgery
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Suk KW, Lee SJ, Kim WS
- KMID: 2110359
- J Korean Ophthalmol Soc.
- 2006 Sep;47(9):1502-1511.
PURPOSE: We report two cases of brothers diagnosed with oculocerebrorenal syndrome after binocular congenital cataract surgery. METHODS: Two brothers who had undergone surgeries for congenital cataracts showed growth retardation, proteinuria, and... -
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- Clinical Characteristics of Arthrogryposis, Renal Tubular Dysfunction, Cholestasis(ARC) Syndrome in Korea
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Lee SM, Kim JH, Lee JS, Han SJ
- KMID: 1627747
- J Korean Soc Pediatr Nephrol.
- 2005 Oct;9(2):222-230.
PURPOSE: ARC syndrome refers to an association of arthrogryposis, renal tubular dysfunction, and cholestasis. The VPS33B gene was recently identified as the causative gene. So far, 41 cases of ARC... -
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- Clinical Study of Hypophosphatemic Rickets
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Lee CJ, Cho HY, Kang JH, Shin CH, Ha IS, Cheong HI, Yang SW, Choi Y
- KMID: 2098814
- J Korean Soc Pediatr Nephrol.
- 2004 Oct;8(2):195-204.
PURPOSE: Hypophosphatemic rickets is a hereditary disease, characterized by hypophosphatemia due to renal phosphate wasting, impaired renal production of 1,25-dihydroxyvitamin D3, rachitic bone deformities and impaired growth. The purpose of... -
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- A Case of the Fanconi Syndrome with Nephrocalcinosis
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Kim YM, Park SS, Lee JS, Kim SY
- KMID: 2098804
- J Korean Soc Pediatr Nephrol.
- 2003 Oct;7(2):234-238.
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... -
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- A Case of Oncogenic Osteomalacia Caused by Chondromyxoid Fibroma
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Oh KW, Kang MI, Lee WY, Lee TK, Chang JH, Suh JP, Cha BY, Lee KW, Son HY, Kang SK, Park JM, Lee KY, Rhee SK, Woo YK
- KMID: 2199572
- J Korean Soc Endocrinol.
- 1999 Dec;14(4):764-770.
Oncogenic osteomalacia is a rare clinicopathological condition. The syndrome is characterized by hypophosphataemic osteomalacia with hyperphosphaturia, low plasma 1,25-dihydroxyvitamin D and normal plasma calcaemia and parathyroid hormone, associated with a... -
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- A Case of Osteosarcoma induced Oncogenic Osteomalacia Detected by MRI
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Lim SK, Song YD, Lee HC, Huh KB, Park KH, Kim KR, Hong SW, Nam JH, Yook JI, Choi BJ, Kim MK, Shin KH
- KMID: 2199472
- J Korean Soc Endocrinol.
- 1999 Jun;14(2):401-409.
Oncogenic osteomalacia is a syndrome characterized by phosphaturia, hypophosphatemia, decreased 1,25-dihydroxyvitamin D level and specific signs and symptoms of osteomalacia. It is associated with the presence of neoplasm originated from... -
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- Two Cases of Pseudohypoparathyroidism
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Hong DE, Lee YK, Kim DU, Jeong DC, Hur JK, Oh CK, Lee IJ, Lee BC
- KMID: 2193878
- J Korean Soc Pediatr Endocrinol.
- 1998 Nov;3(2):219-227.
Pseudohypoparathyroidism(PHP) is a genetic disorder characterized by target cell resistance to the effect of parathyroid hormone(PTH). The disorder is classified into type I a, I b, I... -
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- Changes in renal brush-border sodium-dependent transport systems in gentamicin-treated rats
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Suhl SY, Ahn DW, Kim KR, Kim JY, Park YS
- KMID: 2071512
- Korean J Physiol Pharmacol.
- 1997 Aug;1(4):403-411.
To elucidate the mechanism of gentamicin induced renal dysfunction, renal functions and activities of various proximal tubular transport systems were studied in gentamicin-treated rats (Fisher 344). Gentamicin nephrotoxicity was induced by injecting gentamicin... -
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- A case of Fanconi syndrome
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Lee YW, Lim IS, Kim CH
- KMID: 1945955
- J Korean Pediatr Soc.
- 1993 May;36(5):737-742.
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,... -
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