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Relevant bibliographies by topics / Urethral agenesis

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Academic literature on the topic 'Urethral agenesis'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Urethral agenesis"

1

Delshad, Salahaddin, Hadith Rastad, and Parham Mardi. "Congenital Bladder and Urethral Agenesis: Two Case Reports and Management." Advances in Urology 2020 (September 24, 2020): 1–5. http://dx.doi.org/10.1155/2020/2782783.

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Background. Agenesis of the bladder and urethra is a rare congenital anomaly, with a very few living cases reported in the literature so far. Case Presentation. We are reporting two female patients (3 and 6 years old) with bladder and urethral agenesis who presented with urinary incontinence. In both patients, magnetic resonant imaging (MRI) revealed a case of bladder and urethral agenesis with normal ureters draining into the vagina. Patients underwent a neobladder and conduit creation surgery. The neobladder was constructed from the whole cecum and a part of the ascending colon, followed by

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2

James, R. "Simultaneous penile and urethral agenesis." Urology 43, no. 1 (1994): 130–31. http://dx.doi.org/10.1016/s0090-4295(94)80287-4.

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3

Kafando, Edwige, Boniface Moifo, Landry Mbouche, Derek Ndangoh, Evelyn Mah, and Faustin Mouafo Tambo. "Urethral Duplication with a Cystic Phallic Urethra Associated with a Uterus Didelphys, Partial Agenesis of the Tibia, and an Equinovarus Foot." Case Reports in Radiology 2018 (2018): 1–5. http://dx.doi.org/10.1155/2018/3827820.

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Urethral duplication is a rare congenital malformation, especially in females. It may be associated with complex urogenital malformations, but the association with a cystic phallic urethra and a uterus didelphys is exceptional. We report a case of a newborn with urethral duplication, with the accessory urethra exteriorized by a large cyst, associated with a uterus didelphys and bone malformations. We discuss the clinical, radiographic, and therapeutic aspects as well as a literature review.

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4

O'Connor, Timothy A., Maureen L. Lacour, Edward R. Friedlander, and Ron Thomas. "Penile agenesis associated with urethral and bilateral renal agenesis." Urology 41, no. 6 (1993): 564–65. http://dx.doi.org/10.1016/0090-4295(93)90105-j.

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5

Umama, Huq. "Bladder and Urethral Agenesis: A Report of 2 Cases." Pediatric Surgery in Tropics 1, no. 3 (2024): 167–70. https://doi.org/10.5281/zenodo.12680967.

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Bladder and urethral agenesis are among the rarest congenital anomalies, and toour knowledge, only 27 cases have been reported in English literature until now.The authors treated two such cases in the last one year. The first case wasdiagnosed at 2 months of age, and the second case at 10 months of age. Both werefemales. In The first case ureterosigmoidostomy was done at 1 year of age. Thesecond case had features of chronic kidney disease due to a stenosed ectopic ureter.Therefore, diverting cutaneous ureterostomy was done. Bladder and urethralagenesis are associated with other congenital anom

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6

Rezaie, Mohammad Ali Mohammadzadeh, Ehsan Mansourian, Hossein Rezai Delui, and Negar Mokhtari Amirmajdi. "Bladder and Urethral Agenesis: A Report of Two Cases." Urology 76, no. 1 (2010): 60–61. http://dx.doi.org/10.1016/j.urology.2010.02.006.

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7

Onwuasoanya, Uzodimma E., Olalekan O. Olatise, Nonso O. Epundu, et al. "Incidental diagnosis and treatment of posterior urethral valve in a child with osteogenesis imperfecta: a case report." International Surgery Journal 9, no. 9 (2022): 1640. http://dx.doi.org/10.18203/2349-2902.isj20222244.

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Posterior urethral valve is the commonest cause of both urinary tract obstruction and chronic renal disease in male children. The patients may present with the complications of the disease such as impaired renal function, urinary tract infection, or anaemia. Reports abound about the association of other congenital defects with posterior urethral valve but few studies have reported the association of this disease with osteogenesis imperfecta. An 8-year-old male on management for osteogenesis imperfecta who presented to our facility following renal function test in keeping with impaired renal fu

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8

Liu, Hsin-Mei, Ho-Hsiung Lin, and Sheng-Mou Hsiao. "Impairment of urethral coitus due to mid-urethral sling in a woman with vaginal agenesis." International Urogynecology Journal 30, no. 8 (2019): 1383–85. http://dx.doi.org/10.1007/s00192-019-03972-3.

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9

Aličelebić, Selma, Dina Kapić, and Zakira Mornjaković. "Urinary System Birth Defects in Surgically Treated Infants in Sarajevo Region of Bosnia and Herzegovina." Bosnian Journal of Basic Medical Sciences 8, no. 2 (2008): 126–30. http://dx.doi.org/10.17305/bjbms.2008.2965.

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Congenital anomalies of the urinary system are relatively common anomalies. In Bosnia and Herzegovina there is no existent unique evidence of congenital anomalies and registries. The aim of this study was to obtain the frequency of different urinary tract anomalies types and their sex distribution among cases hospitalized in the Department of Pediatric Surgery of the University of Sarajevo Clinics Centre, Bosnia and Herzegovina, during the period from January 2002 to December 2006. Retrospective study was carried out on the basis of clinical records. Standard methods of descriptive statistics

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10

Öğün, Tunç Cevat, Zekeriya Tosun, Mehmet Arazi, and M. I. Safa Kapicioğlu. "A CASE OF A NEW SYNDROME OR A VARIANT OF THE RARE POPLITEAL PTERYGIUM SYNDROME." Journal of Musculoskeletal Research 05, no. 01 (2001): 73–77. http://dx.doi.org/10.1142/s0218957701000428.

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The popliteal pterygium syndrome is very rare, and is characterized by a congenital popliteal web accompanying the genitourinary, craniofacial, and musculoskeletal anomalies. We described a case of presumably popliteal pterygium syndrome with severe right popliteal web, right renal agenesis, left bifurcated ninth rib, urethral orifice in the vagina, right presacral discoloration resembling A-V malformation, imperforate anus, skin dimple in the left gluteal region, right calcaneovalgus foot with supernumerary digits and aberrant profunda femoris artery. This is the first report of this combinat

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Book chapters on the topic "Urethral agenesis"

1

Fahmy, Mohamed. "Urethral Agenesis." In Congenital Anomalies of the Penis. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-43310-3_23.

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2

"Genital anomalies." In Oxford Handbook of Genitourinary Medicine, HIV, and Sexual Health, edited by Laura Mitchell, Bridie Howe, D. Ashley Price, Babiker Elawad, and K. Nathan Sankar. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780198783497.003.0033.

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Genital anomalies considers both congenital and acquired differences in genital anatomy in both men and women. Clinicians performing genital examinations will frequently encounter many of these in their practice, and within this chapter each anomaly is succinctly described and for many the appropriate management is subsequently outlined. In men, the following differences are included: epispadias, hypospadias, lymphocele, paraphimosis, Peyronie’s disease, priapism, phimosis, spermatoceles and epididymal cysts, urethral channels, and varicocele. In women: Bartholin gland pathology (cysts and abs

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3

Khadir, Mohammed Mohsin. "Pediatric Genitourinary Radiology." In Ultrasound Guided Procedures and Radiologic Imaging for Pediatric Anesthesiologists, edited by Anna Clebone, Joshua H. Finkle, and Barbara K. Burian. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190081416.003.0013.

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Chapter 13 examines radiologic images for common and uncommon pediatric genitourinary disorders. These include pediatric congenital disorders such as renal agenesis, autosomal recessive polycystic kidney disease, multicystic dysplastic kidney, horseshoe kidney/cross-fused ectopia, prune belly syndrome, congenital uteropelvic junction obstruction, vesicoureteral reflux, duplicated collecting system, ureterocele, urachal anomalies, bladder exstrophy, and posterior urethral valves. The chapter goes on to look at neuroblastoma and Wilms tumor. Reproductive disorders are also examined, such as ovar

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