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abnormal presence of amino acids in the urine; usually a symptom of metabolic defects

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1. 化学療法関連腎毒性および腎不全患者における用量調整 chemotherapy related nephrotoxicity and dose modification in patients with renal insufficiency
2. 正常妊娠における腎臓および尿路の生理機能 renal and urinary tract physiology in normal pregnancy
3. 尿細管間質性腎炎とブドウ膜炎（TINU症候群） tubulointerstitial nephritis and uveitis tinu syndrome
4. イホスファミドの腎毒性 ifosfamide nephrotoxicity
5. 腎疾患の診断における尿検査 urinalysis in the diagnosis of kidney disease

Cystinosis: renal glomerular and renal tubular function in relation to compliance with cystine-depleting therapy.

Nesterova G1, Williams C, Bernardini I, Gahl WA.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2015 Jun;30(6):945-51. doi: 10.1007/s00467-014-3018-x. Epub 2014 Dec 20.
BACKGROUND AND OBJECTIVES: Nephropathic cystinosis is a lysosomal storage disorder characterized by renal tubular Fanconi syndrome in infancy and glomerular damage leading to renal failure at ∼10 years of age. Therapy with the cystine-depleting agent cysteamine postpones renal failure, but the de
PMID 25526929

Transient renal Fanconi syndrome in a Chihuahua exposed to Chinese chicken jerky treats.

Hooijberg EH1, Furman E, Leidinger J, Brandstetter D, Hochleithner C, Sewell AC, Leidinger E, Giger U.
Tierarztliche Praxis. Ausgabe K, Kleintiere/Heimtiere.Tierarztl Prax Ausg K Kleintiere Heimtiere.2015 May 13;43(3). [Epub ahead of print]
Transient Fanconi syndrome without azotemia was diagnosed in a dog and was associated with ingestion of Chinese chicken jerky treats. Fanconi syndrome is a proximal renal tubular defect and a diagnosis was made based upon severe glucosuria with normoglycemia, and severe generalized aminoaciduria. Th
PMID 25966748

Nephropathic Cystinosis Presenting as Renal Fanconi Syndrome without Glycosuria.

Kanthila J1, Dsa S1, Bhat KG1.
Journal of clinical and diagnostic research : JCDR.J Clin Diagn Res.2015 Mar;9(3):SD05-6. doi: 10.7860/JCDR/2015/10875.5692. Epub 2015 Mar 1.
Renal Fanconi syndrome is diagnosed by its cardinal features of glycosuria without diabetes, aminoaciduria, phosphaturia, and renal tubular acidosis. It is often associated with hypokalaemia, hypophosphatemia and rickets. We report a seven-year-old boy with nephropathic cystinosis who presented with
PMID 25954677

Multiple bone fracture due to Fanconi's syndrome in primary Sjögren's syndrome complicated with organizing pneumonia.

Nakamura Hideki,Kita Junko,Kawakami Atsushi,Yamasaki Satoshi,Ida Hiroaki,Sakamoto Noriho,Furusu Akira,Eguchi Katsumi
Rheumatology international 30(2), 265-267, 2009-12
… A 66-year-old woman showing renal dysfunction with elevated serum alkaline phosphatase and anti-SS-A antibody was admitted. … Fanconi's syndrome was diagnosed by renal tubular acidosis along with renal glucosuria or aminoaciduria and multiple bone fractures on bone scintigraphy. …
NAID 120001629865

田中幸代,鈴川純子,荒木敦,今井雄一郎,高屋淳二,谷内昇一郎,蓮井正史,金子一成
日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 21(2), 182-187, 2008-11-15
　バルプロ酸 (valproate: VPA) によるFanconi症候群 (以下，本症) を呈していた22歳の重症心身障害者が，肺炎を契機に急性腎不全を合併した。本症に急性腎不全を合併した報告は，検索した範囲では見あたらなかった。　患者は生後8ヵ月からWest症候群の治療としてVPAを投与されており，定期的な血液，尿検査を受けていたが，21歳7ヵ月から低尿酸血症を，21歳9ヵ月から尿糖・蛋白尿を …
NAID 10025170507

丸山健一,渡辺美緒,関満,畠山信逸,黒岩実,鬼形和道
日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 19(2), 152-155, 2006-11-15
　本邦第２例と思われるARC症候群の１女児例を経験した。在胎38週，2,466gで出生したが，生下時より両側足関節の拘縮を指摘されていた。閉塞性黄疸が出現したため１ヵ月時に当院へ転院となった。胆道閉鎖症は否定されたが，蛋白尿，糖尿，汎アミノ酸尿が見られた。さらに，中枢神経系合併症（脳梁低形成，多小脳回，難聴）も認められた。ペルオキシソーム病，ミトコンドリア病は否定的であり，臨床症状よりARC症候群 …
NAID 10025700853