Adult idiopathic renal Fanconi syndrome: A case report
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Dae Jin | - |
dc.contributor.author | Jang, Ki-Seok | - |
dc.contributor.author | Kim, Gheun-Ho | - |
dc.date.accessioned | 2021-07-30T04:58:14Z | - |
dc.date.available | 2021-07-30T04:58:14Z | - |
dc.date.created | 2021-05-13 | - |
dc.date.issued | 2018-03 | - |
dc.identifier.issn | 1738-5997 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/2404 | - |
dc.description.abstract | 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 disorders, and modern molecular genetics may explain the etiology of previous idiopathic cases of RFS. Here, we report the case of a 52-year-old woman with RFS whose etiology could not be identified. She presented with features of phosphaturia, renal glucosuria, aminoaciduria, tubular proteinuria, and proximal renal tubular acidosis. Her family history was unremarkable, and previous medications were nonspecific. Her bone mineral density was compatible with osteoporosis, serum intact parathyroid hormone level was mildly elevated, and 25(OH) vitamin D level was insufficient. Her blood urea nitrogen and serum creatinine levels were 8.4 and 1.19 mg/dL, respectively (estimated glomerular filtration rate, 53 mL/min/1.73 m2). Percutaneous renal biopsy was performed but revealed no specific renal pathology, including mitochondrial morphology. No mutation was detected in EHHADH gene. We propose the possibility of involvement of other genes or molecules in this case of adult RFS. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | Korean Society of Electrolyte and Blood Pressure Research | - |
dc.title | Adult idiopathic renal Fanconi syndrome: A case report | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Jang, Ki-Seok | - |
dc.contributor.affiliatedAuthor | Kim, Gheun-Ho | - |
dc.identifier.doi | 10.5049/EBP.2018.16.2.19 | - |
dc.identifier.scopusid | 2-s2.0-85068222532 | - |
dc.identifier.bibliographicCitation | Electrolyte and Blood Pressure, v.16, no.2, pp.19 - 22 | - |
dc.relation.isPartOf | Electrolyte and Blood Pressure | - |
dc.citation.title | Electrolyte and Blood Pressure | - |
dc.citation.volume | 16 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 19 | - |
dc.citation.endPage | 22 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.identifier.kciid | ART002446103 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.subject.keywordPlus | 25 hydroxyvitamin D | - |
dc.subject.keywordPlus | calcitriol | - |
dc.subject.keywordPlus | creatinine | - |
dc.subject.keywordPlus | lactic acid plus magnesium chloride plus sodium bicarbonate plus sodium chloride | - |
dc.subject.keywordPlus | parathyroid hormone | - |
dc.subject.keywordPlus | adult | - |
dc.subject.keywordPlus | aminoaciduria | - |
dc.subject.keywordPlus | Article | - |
dc.subject.keywordPlus | bone density | - |
dc.subject.keywordPlus | case report | - |
dc.subject.keywordPlus | clinical article | - |
dc.subject.keywordPlus | creatinine blood level | - |
dc.subject.keywordPlus | estimated glomerular filtration rate | - |
dc.subject.keywordPlus | Fanconi renotubular syndrome | - |
dc.subject.keywordPlus | female | - |
dc.subject.keywordPlus | human | - |
dc.subject.keywordPlus | human tissue | - |
dc.subject.keywordPlus | idiopathic disease | - |
dc.subject.keywordPlus | kidney biopsy | - |
dc.subject.keywordPlus | kidney tubule acidosis | - |
dc.subject.keywordPlus | middle aged | - |
dc.subject.keywordPlus | parathyroid hormone blood level | - |
dc.subject.keywordPlus | phosphaturia | - |
dc.subject.keywordPlus | proteinuria | - |
dc.subject.keywordPlus | urea nitrogen blood level | - |
dc.subject.keywordPlus | vitamin blood level | - |
dc.subject.keywordAuthor | EHHADH gene | - |
dc.subject.keywordAuthor | Idiopathic Fanconi syndrome | - |
dc.subject.keywordAuthor | Osteoporosis | - |
dc.subject.keywordAuthor | Phosphaturia | - |
dc.subject.keywordAuthor | Renal tubular acidosis | - |
dc.identifier.url | https://enbpr.org/DOIx.php?id=10.5049/EBP.2018.16.2.19 | - |
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