Results 1 to 10 of about 32,063 (145)

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

Urology 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
exaly   +5 more sources

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

African 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, Iniofon Clement Akpaette, Owolabi Oni, Igwe Arua Obasi, Ibukunolu Olufemi Ogundele, Abdulhafiz Adesunkanmi, Oluwaseun Abioye Oyinloye, Ademola Olusegun Talabi, Oludayo Adedapo Sowande, Olusanya Adejuyigbe   +9 more
doaj   +3 more sources

Penile agenesis: a case report

Journal 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.
Fatma Hilal Yilmaz, Nuriye Tarakci
exaly   +4 more sources

Successful conservative management of isolated hemiscrotal agenesis: case report [PDF]

Urology Case Reports
Hemiscrotal agenesis is an extremely rare congenital anomaly characterized by unilateral absence of scrotal skin with preserved midline raphe. Optimal management, particularly conservative approaches in isolated cases without cryptorchidism, remains ...
Mariam Marzouki, Yosra Ben Ahmed, Rim Ezzine, Mariem Boukattaya, Said Jlidi   +4 more
doaj   +2 more sources

A variant of Zinner syndrome with ectopic ureteral insertion into the seminal vesicle [PDF]

Radiology Case Reports
Zinner syndrome comprises a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction, which can be accompanied by additional abnormalities of the genitourinary tract in some cases.
Ali Al-Smair, MD, Muhannad M. Mahmoud, MD, Murad T. Attal, MD, Israa N. Alzawawi, MD   +3 more
doaj   +2 more sources

A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula

Radiology Case Reports, 2022
Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder.
Behnam Kian, MD, Saeed Esmaeilian, MD, Mehrdad Kayedi, MD   +2 more
doaj   +1 more source

A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency

Case Reports in Pediatrics, 2020
Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and ...
R. El Qadiry, A. Lalaoui, H. Nassih, A. Bourrahouat, I. Ait Sab   +4 more
doaj   +1 more source

A rare association between crossed fused renal ectopia, urethral stricture, bilateral cryptorchidism, and sub-coronal hypospadias in a non-syndromic 6-year-old child

Journal of Pediatric Surgery Case Reports, 2023
Introduction: From asymptomatic ectopic kidneys to potentially fatal renal agenesis, congenital abnormalities of the kidney and urinary tract (CAKUT) encompass a wide variety of anomalies (bilateral).
Oadi N. Shrateh, Afnan W.M. Jobran, Saja Jaber, Ahmad Kahla, Mohammad Shker, Wael Abu Arafeh   +5 more
doaj   +1 more source

Penile Agenesis

Indian 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   +1 more source

CONGENITAL SEGMENTAL DILATATION OF SIGMOID COLON, PENILE AGENESIS AND UMBLICAL CORD HERNIA - A NEW ASSOCIATION

Journal of the Dow University of Health Sciences, 2009
Congenital segmental dilatation of the colon, penile agenesis and umbilical cord hernia are individually rare congenital malformations. An association between all three malformations has not been previously reported.
Muhammad Talat Mehmood, Farhan Shahzad, Muhammad Sajjad Ashraf, Muhammad Shahab Athar, Javed Ahmad   +4 more
doaj   +4 more sources