先天性水腎症
WordNet
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
- accumulation of urine in the kidney because of an obstruction in the ureter
PrepTutorEJDIC
- (病気・身体的欠陥など)生まれつきの,先天的な
UpToDate Contents
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- 1. 胎児水腎症の概要 overview of fetal hydronephrosis
- 2. 尿路閉塞および水腎症の臨床症状および診断 clinical manifestations and diagnosis of urinary tract obstruction and hydronephrosis
- 3. 原発性膀胱尿管逆流の臨床症状、診断、および経過 clinical presentation diagnosis and course of primary vesicoureteral reflux
- 4. 先天性腎尿路異常(CAKUT)の概要 overview of congenital anomalies of the kidney and urinary tract cakut
- 5. 腎性尿崩症の治療 treatment of nephrogenic diabetes insipidus
English Journal
- Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT).
- Bartram MP, Höhne M, Dafinger C, Völker LA, Albersmeyer M, Heiss J, Göbel H, Brönneke H, Burst V, Liebau MC, Benzing T, Schermer B, Müller RU.SourceDepartment 2 of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
- Journal of molecular medicine (Berlin, Germany).J Mol Med (Berl).2013 Jun;91(6):739-48. doi: 10.1007/s00109-013-1000-x. Epub 2013 Jan 24.
- MicroRNAs have emerged as essential regulators of gene expression and may play important roles in a variety of human disorders. To understand the role of microRNA-mediated gene regulation in the kidney, we deleted the microRNA-processing enzyme Dicer in developing renal tubules and parts of the uret
- PMID 23344677
- Renal pelvis rupture in a kidney with ureteropelvic junction obstruction and extrarenal calyces.
- Ransford G, Young E, Castellan M, Labbie A.SourceUniversity of Miami, Miller School of Medicine, 1400 NW 10th Ave Suite 501, Miami, FL 33136, USA. Electronic address: gransford@med.miami.edu.
- Journal of pediatric urology.J Pediatr Urol.2013 Jun;9(3):e127-30. doi: 10.1016/j.jpurol.2012.12.018. Epub 2013 Feb 23.
- The extrarenal calyx (ERC) is a rare congenital anomaly, associated with various other abnormalities of the urogenital system. We report a unique case of ERC in a solitary functioning kidney with a massively dilated pelvis that developed spontaneous rupture. A dismembered pyeloplasty was performed a
- PMID 23462383
- In utero oxcarbazepine and a withdrawal syndrome, anomalies, and hyponatremia.
- Rolnitsky A, Merlob P, Klinger G.SourceNeonatology Department, Schneider Children's Medical Center of Israel, Petah Tikva, Israel; Sackler School of Medicine, Tel Aviv University, Petah Tikva, Israel.
- Pediatric neurology.Pediatr Neurol.2013 Jun;48(6):466-8. doi: 10.1016/j.pediatrneurol.2013.02.012.
- Oxcarbazepine is an antiepileptic agent that has been used during pregnancy, although its safety during pregnancy has not been sufficiently established. This article presents an infant born with renal and cardiac malformations who developed a withdrawal syndrome and hyponatremia following in utero e
- PMID 23668873
Japanese Journal
- 症例報告 先天性水腎症および巨大尿管症を伴った片側性異所性尿管症のイヌの一症例
- 画像上腎嚢胞性疾患との鑑別が困難であった先天性巨大水腎症の1例
- 先天性水腎症(腎盂尿管移行部狭窄) (小児の治療指針) -- (腎・尿路)
Related Links
- [Program of early nephro-urologic management of children with congenital hydronephrosis] Pol Merkur Lekarski. 2009 Apr; 26(154):273-5. [Pol Merkur Lekarski. 2009] Apoptosis of renal tubular cells in congenital hydronephrosis.
- The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a ...
★リンクテーブル★
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- 英
- congenital hydronephrosis
- 関
- 水腎症
病因
- 参考1
- 胎内において水腎症をきたす原因
参考
- 1. [charged] Overview of antenatal hydronephrosis - uptodate [1]
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- 関
- congenital、congenitally
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