Results 11 to 20 of about 1,659 (187)
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 +4 more
doaj +5 more sources
A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula [PDF]
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 +2 more
doaj +2 more sources
Rare Phallus Malformations in Children [PDF]
Iranian Journal of Pediatric Surgery, 2016 Introduction: Penile agenesis (PA) and diphallus (DP) are extremely rare genital anomaly in children. Numerous associated anomalies have been described with these malformations. These patients need several investigations and finally surgical intervention.
Javad Ghoroubi +2 more
doaj +3 more sources
Penile agenesis: A case report
Pediatric Urology Case Reports, 2014 Absence of the penis is a rare congenital anomaly of the male infant that may be associated with other congenital anomalies. Management in the last two decades has changed from initial female gender assignment to penile reconstruction procedures.
Hussaini Yusuf Maitama +2 more
openalex +2 more sources
A variant of Zinner syndrome with ectopic ureteral insertion into the seminal vesicle [PDF]
Radiology Case ReportsZinner 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 +3 more
doaj +2 more sources
An unusual presentation of urethral duplication presenting with chronic bladder retention, left scrotal transposition and left renal agenesis [PDF]
International Brazilian Journal of Urology, 2018 Introduction and objective Urethral duplication is a rare congenital anomaly, with roughly 200 cases reported in the literature (1). It is more frequent in males, with few cases reported in females.
Antonio Macedo Jr. +7 more
doaj +4 more sources
Phalloplasty and urethroplasty in a boy with penile agenesis
Journal of Pediatric Urology, 2012 New concepts in ambiguous genitalia have questioned the strategy of female gender reassignment in cases of penile agenesis. Hence, we present a video of the construction of a phallus according to the De Castro technique as an alternative approach for this devastating condition.A 12-year-old boy with congenital penile agenesis and posterior urethra ...
Roberto De Castro +4 more
openalex +4 more sources
Mymensingh medical journal : MMJ, 2011 Penile agenesis (PA) is an extremely rare congenital anomaly with profound surgical and psychosocial consequences. Only seventy five cases have been reported in the literature, the highest age of presentation known seven years. We present a twenty six years old otherwise normal aphallic male with attraction to female sex and night emission through anus.
Mahfuza Momen +5 more
openalex +2 more sources
"Penile Agenesis- An Extremely Rare Urogenital Anomaly"
International Journal of Current Research and Review, 2018 Mayukh Chakraborty +18 more
openalex +2 more sources