 Urogenital Abnormalities
"Urogenital Abnormalities" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female.
| Descriptor ID |
D014564
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| MeSH Number(s) |
C12.706 C13.351.875 C16.131.939
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| Concept/Terms |
Urogenital Abnormalities- Urogenital Abnormalities
- Abnormality, Urogenital
- Urogenital Abnormality
- Genitourinary Abnormalities
- Abnormalities, Genitourinary
- Abnormality, Genitourinary
- Genitourinary Abnormality
- Abnormalities, Urogenital
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Below are MeSH descriptors whose meaning is more general than "Urogenital Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Urogenital Abnormalities".
This graph shows the total number of publications written about "Urogenital Abnormalities" by people in this website by year, and whether "Urogenital Abnormalities" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 | | 2002 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2004 | 0 | 2 | 2 | | 2005 | 2 | 0 | 2 | | 2006 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2011 | 2 | 1 | 3 | | 2012 | 1 | 0 | 1 | | 2014 | 2 | 1 | 3 | | 2015 | 3 | 0 | 3 | | 2016 | 0 | 1 | 1 | | 2017 | 3 | 0 | 3 | | 2018 | 5 | 1 | 6 | | 2020 | 1 | 0 | 1 | | 2021 | 2 | 0 | 2 | | 2022 | 3 | 0 | 3 | | 2023 | 3 | 0 | 3 | | 2024 | 1 | 0 | 1 | | 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.
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Forster CS, Wood AC, Davis-Rodriguez S, Desai S, Chang PW, Tchou MJ, Morrison JM, Hamdy RF, Vemulakonda V, Brady PW, Abou Zeid C, Wallace SS. Variability in Treatment of UTIs in Children With Genitourinary Anomalies in Children's Hospitals. Hosp Pediatr. 2025 Apr 01; 15(4):309-317.
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Forster CS, Wood AC, Davis-Rodriguez S, Chang PW, Desai S, Tchou M, Morrison JM, Mudd JD, Casey BD, Trevisanut V, Hamdy RF, Vemulakonda V, Brady PW, Wallace SS. Frequency of Treatment Failure of UTIs in Children With Congenital Urinary Tract Anomalies. Hosp Pediatr. 2024 03 01; 14(3):189-196.
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Harris KT, Kong L, Vargas M, Hou V, Pyrzanowski JL, Desanto K, Wilcox DT, Wood D. Considerations and Outcomes for Adolescents and Young Adults With Cloacal Anomalies: A Scoping Review of Urologic, Colorectal, Gynecologic and Psychosocial Concerns. Urology. 2024 01; 183:264-273.
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Wehrli LA, Reppucci ML, Woodfield K, Ketzer J, Rieck JM, Cooper EH, De La Torre L, Pena A, Bischoff A, Alaniz VI. Fertility concerns and outcomes in females with anorectal malformations. Pediatr Surg Int. 2023 Jul 09; 39(1):228.
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Harris KT, Wilcox DT. Commentary to Partial Urogenital Mobilization in Cloacal Malformation: Is it a Viable Option? J Pediatr Urol. 2023 10; 19(5):520.
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Reppucci ML, Alaniz VI, Wehrli LA, Torre L, Wood D, Wilcox DT, Appiah LC, Pe?a A, Bischoff A. Reproductive and Family Building Considerations for Female Patients with Anorectal And Urogenital Malformations. J Pediatr Surg. 2023 Aug; 58(8):1450-1457.
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Murphey K, George PE, Pencheva B, Porter CC, Wechsler SB, Gambello MJ, Li H. Acute myeloid leukemia and dilated cardiomyopathy in a pediatric patient with D-2-hydroxyglutaric aciduria type I. Am J Med Genet A. 2022 09; 188(9):2707-2711.
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Sanderson KR, Shih WV, Warady BA, Claes DJ. Severe Fetal CAKUT (Congenital Anomalies of the Kidneys and Urinary Tract), Prenatal Consultations, and Initiation of Neonatal Dialysis. Am J Perinatol. 2024 05; 41(S 01):e156-e162.
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Dorafshar AH, Hamidian Jahromi A, Horen SR, Schechter LS, Johannesson L, Testa G, Hertl M, Dewdney S, Aschkenasy J, Wood-Molo M, Brincat C, Cherullo E, Behel JM, Hebert C, Shulman R, Bassi S, Alecci AT, Konety B. Strategic Planning and Essential Steps for Establishing a Uterine Transplant and Rehabilitation Program: From Idea to Reality. Ann Surg. 2022 07 01; 276(1):74-80.
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Lemire G, Zheng B, Ediae GU, Zou R, Bhola PT, Chisholm C, de Nanassy J, Lo B, Wang C, Shril S, El Desoky S, Shalaby M, Kari JA, Wang X, Kernohan KD, Boycott KM, Hildebrandt F, Sawyer SL. Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. Am J Med Genet A. 2021 10; 185(10):3005-3011.
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