Zobrazeno 1 - 10
of 64
pro vyhledávání: '"renal dysgenesis"'
Publikováno v:
South African Journal of Radiology, Vol 27, Iss 1, Pp e1-e5 (2023)
Tubulocystic anomalies of the mesonephric duct (MND) are a rare group of related entities with a perplexing clinical presentation. Ultrasound is a useful screening investigation, which can help identify a dysplastic kidney or point to renal agenesis
Externí odkaz:
https://doaj.org/article/c766629872664b2189166a4e713b4e58
Publikováno v:
Radiology - Practice. :161-170
Herlin — Werner — Wunderlich syndrome or OHVIRA (Obstructed hemivagina and ipsilateral renal anomaly) is a rare type of uterine and vaginal doubling defect (0,1 – 10,0 % of all uterine abnormalities) which is characterized by a triad of symptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26a8f86373c73b3afc5272748638117c
https://doi.org/10.52560/2713-0118-2021-5-161-170
https://doi.org/10.52560/2713-0118-2021-5-161-170
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 20, Iss 1, Pp 59-63 (2015)
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome is an autosomal dominant disease caused by mutations in the GATA3 gene on chromosome 10p15. We identified a patient diagnosed with hypoparathyroidism who also had a family hist
Externí odkaz:
https://doaj.org/article/af10003609124e238c6ccbde4fbdb0b0
Autor:
Jonathan Gerber, Mary Taylor Winsten, Yuan Yuan Gong, Katherine L. O'Flynn O'Brien, Vinaya Bhatia, Jennifer E. Dietrich, Mona Homafar
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 34:154-160
Study Objective To characterize the prevalence of Mullerian anomalies (MAs) among patients with renal anomalies (RAs). Design, Setting, Participants, Interventions, and Main Outcome Measures A retrospective chart review of female patients with RAs wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eba7f2724a1b6fa47e6b5ff2308dca1
https://doi.org/10.1016/j.jpag.2020.11.015
https://doi.org/10.1016/j.jpag.2020.11.015
Akademický článek
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Kniha
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Publikováno v:
Anales de Pediatría, Vol 80, Iss 1, Pp 51-54 (2014)
Resumen: Las valvas ureterales son malformaciones muy poco frecuentes, con una incidencia de uno de cada 5.000-8.000 nacidos vivos. Las malformaciones relacionadas con la esfera urológica se asocian en un 50% de los casos según la literatura actual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abc20b8ff9375b2d5490ad7a18270a7f
http://www.sciencedirect.com/science/article/pii/S1695403313001999
http://www.sciencedirect.com/science/article/pii/S1695403313001999
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 87:180-183
Branchio-oto-renal syndrome, first defined in 1976, is an autosomal dominant disorder characterized by anomalies of the external, middle, and inner ear in association with preauricular sinuses, branchial cleft anomalies, and varying degrees of renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be117d93df552e1054c7255b215a8dc4
https://doi.org/10.1016/s1079-2104(99)70270-2
https://doi.org/10.1016/s1079-2104(99)70270-2
Publikováno v:
Journal of Urology. 159:217-221
We describe the differential points in the diagnosis of the combination of renal dysgenesis, Gartner's duct cyst and ipsilateral müllerian duct obstruction. Various imaging studies and urological procedures were performed. We report our experience i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ff70e90a33e3978d60712553add477
https://doi.org/10.1016/s0022-5347(01)64071-0
https://doi.org/10.1016/s0022-5347(01)64071-0
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 10:197-202
腎の形態・機能障害と先天性半身肥大を伴う腹部腫瘍の2例を報告した。1例目は10歳女子で左側先天性半身肥大と両側性海綿腎を有す。小さい右腎は高度の機能不全をきたし，大きい左腎
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64e1e1a0e9ec503cc120923f854677e3
https://doi.org/10.3165/jjpn.10.197
https://doi.org/10.3165/jjpn.10.197