| Item type |
☆紀要論文 / Departmental Bulletin Paper(1) |
| 公開日 |
2016-06-14 |
| タイトル |
|
|
タイトル |
<Case Reports> A patient with renal hypouricemia and acute renal failure after exercise in whom URAT1 gene mutation was demonstrated |
|
言語 |
en |
| 著者 |
Enya, Takuji
Sugimoto, Keisuke
Miyazawa, Tomoki
Nishi, Hitomi
Miyazaki, Kohei
Okada, Mitsuru
Takemura, Tsukasa
|
| 言語 |
|
|
言語 |
eng |
| キーワード |
|
|
主題 |
renal hypouricemia, acute renal failure, exercise, URAT1, GLUT9 |
| 資源タイプ |
|
|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
departmental bulletin paper |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kinki University Faculty of Medicine |
| 版 |
|
|
出版タイプ |
VoR |
|
出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| 出版者 名前 |
|
|
出版者 |
Kinki University Medical Association |
| 書誌情報 |
en : ACTA MEDICA KINKI UNIVERSITY
巻 40,
号 2,
p. 39-42,
発行日 2015-12
|
| ISSN |
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収録物識別子タイプ |
ISSN |
|
収録物識別子 |
03866092 |
| 抄録 |
|
|
内容記述タイプ |
Abstract |
|
内容記述 |
[Abstract] Patients with the disease entity termed acute renal failure with severe loin pain and patchy renal ischemia after anaerobic exercise (ALPE) manifests non-oliguric renal failure, usually accompanied by few urinary abnormalities such as hematuria and proteinuria. This condition, diagnosed by the demonstration of hypouricemia in addition to these features, usually responds well to conservative treatment. However, differentiation from other renal disorders occasionally proves difficult, which can lead to unnecessary steroid administration and renal biopsy. In the patient reported here, acute glomerulonephritis (AGN) was initially suspected based on his course and urinalysis findings, although typical AGN symptoms such as oliguria, edema, and hypertension were absent. After the detection of hypouricemia, renal hypouricemia was added to the clinical picture. URAT1 gene mutation (W258X, homozygote) was demonstrated by gene analysis. The patient's mother was heterozygous for mutation at the same site. |
| フォーマット |
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|
内容記述タイプ |
Other |
|
内容記述 |
application/pdf |
AA0050842X-20151200-0039.pdf (180.9 kB)
