WordNet

either of two bean-shaped excretory organs that filter wastes (especially urea) from the blood and excrete them and water in urine; "urine passes out of the kidney through ureters to the bladder"

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Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.

de la Dure-Molla M1, Quentric M, Yamaguti PM, Acevedo AC, Mighell AJ, Vikkula M, Huckert M, Berdal A, Bloch-Zupan A.
Orphanet journal of rare diseases.Orphanet J Rare Dis.2014 Jun 14;9:84. doi: 10.1186/1750-1172-9-84.
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as nephrocalcinosis in Enamel Renal Syndrome (ERS, MIM#204
PMID 24927635

Challenges in the management of bilateral single-system ectopic ureters in male infants.

O'Connor E1, Peeraully R1, Shepherd G2, Shenoy M1.
Urology.Urology.2014 Jun;83(6):1373-7. doi: 10.1016/j.urology.2013.12.047. Epub 2014 Mar 5.
OBJECTIVE: To describe our experience of managing bilateral single-system ectopic ureters in boys.METHODS: We discuss difficulties in diagnosis, importance of appropriate preoperative imaging, and the individualized surgical management for this rare congenital malformation.RESULTS: The first patient
PMID 24612757

Unilateral hypoplastic kidney - a novel highly penetrant feature of familial juvenile hyperuricaemic nephropathy.

Plumb LA, Marlais M, Bierzynska A, Martin H, Brugger K, Abbs S, Saleem MA1.
BMC nephrology.BMC Nephrol.2014 May 9;15:76. doi: 10.1186/1471-2369-15-76.
BACKGROUND: Familial juvenile hyperuricaemic nephropathy is a rare inherited nephropathy with genetic heterogeneity. Categorised by genetic defect, mutations in uromodulin (UMOD), renin (REN) and hepatocyte nuclear factor-1β (HNF-1β) genes as well as linkage to chromosome 2p22.1-21 have previously
PMID 24886545