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A rare presentation: Penile agenesis, vesicoureteral reflux, and rectovesical fistula in a newborn [PDF]

open access: goldUrology Case Reports, 2019
The penis is an important organ in fertility, urinary and psychosexual structure of males. Complete penile agenesis is a rare congenital genitourinary anomaly and is usually associated with other malformations such as gastrointestinal, cardiac, and ...
Müslim Yurtçu
doaj   +5 more sources

Penile agenesis associated with anorectal malformation and bilateral renal agenesis: A case report and a review of the literature [PDF]

open access: goldAfrican Journal of Paediatric Surgery
Penile agenesis is complete absence of the penis in an otherwise normal phenotypic and genotypic male at birth that results from failure of development of the genital tubercle.
Collins Chijioke Adumah   +9 more
doaj   +5 more sources

Penile agenesis

open access: diamondJournal of Indian Association of Pediatric Surgeons, 2005
Penile agenesis is an extremely rare disorder with profound urological and psychological consequences. The goal of treatment is an early female gender assignment and feminizing reconstruction of the perineum.
Bangroo A, Khetri Ramji, Tiwari Sashi
doaj   +3 more sources

Penile Agenesis [PDF]

open access: hybridIndian Journal of Plastic Surgery, 1977
This rare congenital znomaly had been reported in only 37 cases The condition is a result of incomplete development of the genital tubercle. Other urogenital anomaly should be investigated thoroughly.
I. J. Gupta, Ramesh Chandra
doaj   +3 more sources

Penile agenesis: a case report

open access: diamondJournal of Contemporary Medicine, 2020
Penile agenesis is a rarely seen congenital anomaly with dramatic psychological outcomes. In more than half of the patients, other genitourinary anomalies can accompany penile agenesis.
Nuriye Tarakçı   +2 more
doaj   +4 more sources

Aphallia (Penile agenesis): A preliminary report of three cases

open access: diamondPediatric Urology Case Reports, 2017
Aphallia (penile agenesis) is an extremely rare abnormality with the reported incidence of 1 in 30 million births. The cause of this anomaly is associated with no genital tubercle formation or its development impairment. The majority of patients have 46XY Karyotype. The scrotum, testes and testicular function are usually normal.
Prashant Sadashiv Patil   +6 more
core   +4 more sources

Penile agenesis (afallia) in pueros

open access: diamondRussian Journal of Pediatric Surgery, 2021
Introduction. Penile agenesis (aphallia) is an extremely rare congenital defect characterized by the complete absence of the penis in a child with a male karyotype 46XY.Material. The analysis of the literature on keywords in the Pubmed and Medline databases was carried out.Results.
И. М. Каганцов   +4 more
openalex   +2 more sources

22q11 deletion syndrome and urogenital manifestationsA clinicopathological case report and review of the literatureM.Vachette MD*, GE.Grant MD*, J.Bouquet de Joliniere MD.PhD*, M. Jotterand MD** N.Ben Ali MD*, A.Feki MD.PhD * and R.Brugger MD.*Department of gynecology and obstetrics, HFR, Fribourg, Switzerland.** Institute of pathology, CHUV, Lausanne, Switzerland. [PDF]

open access: yesFrontiers in Medicine, 2016
Background: Deletion in the chromosomal region 22q11 results from the abnormal development of the third and fourth pharyngeal pouches during embryonic life and presents an expansive phenotype with more than 180 clinical features described that involve ...
Jean Bouquet De Jolinière
doaj   +3 more sources

De Castro falloplasty of the with penile agenesis

open access: diamondRussian Journal of Pediatric Surgery, Anesthesia and Intensive Care, 2021
Introduction. Penile agenesis (aphallia) is an extremely rare congenital disorder. At present, about 100 cases of the anomaly have been described around the world. The incidence of this congenital anomaly is estimated to be one case per 2030 million births.
И. М. Каганцов   +2 more
openalex   +3 more sources

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