Results 21 to 30 of about 232 (115)

Congenital aphallia associated with congenital urethrorectal fistula: A rare case report. [PDF]

Medicine (Baltimore), 2022
Abstract Rationale: Aphallia is an extremely rare congenital malformation of unknown cause, with few reports in the literature. It is usually associated with other urogenital and gastrointestinal anomalies and is believed to be a result of either the absence of a genital tubercle or chromosome polymorphism. Herein, we
Luo SS, Yang Z, Ma N, Wang WX, Chen S, Wu Q, Qu SW, Li YQ.   +7 more
europepmc   +3 more sources

A Rare case of Aphallia [PDF]

Journal of Pediatric Nephrology, 2016
. Aphallia (total absence of penis) is an extremely rare abnormality that can be part of the urorectal septum malformation sequence. We are reporting a 40-day-old boy who was referred to our nephrology clinic due to the absence of the penis and urinating through the rectum. He was born to a 17-year-old mother and a 24-year-old father, and was delivered
Moghtaderi, Mastaneh, Boroomand, Maryam, Kajbafzadeh, Abdolmohammad, Arshadi, Hamid, Ghohestani, Mohammad, Mehdizadeh, Mehrzad   +5 more
openaire   +2 more sources

Unveiling a Unique Posterior Cloaca Variant: Expanding the Spectrum [PDF]

European Journal of Pediatric Surgery Reports
A posterior cloacal variant is a congenital malformation where a urogenital sinus terminates anterior to a normally placed anus. These are rare malformations with highly variable anatomy.
Tarlia Rasa Govender, Emanuele Trovalusci, Andre Theron, Chris Westgarth-Taylor, Giulia Brisighelli   +4 more
doaj   +2 more sources

Application of Yang-Monti’s Principle as Part of Reconstructive Procedures for Complex Pediatric Surgical Cases: A Single-center Study Case Series [PDF]

Journal of Indian Association of Pediatric Surgeons
Introduction: Reconstructive surgery in pediatric patients often presents unique challenges due to anatomical and physiological differences compared to adults. The Yang-Monti principle, first described for urological reconstruction, has gained widespread
Hemangi Ramchandra Athawale, Lamia Inayat, Viral Bhatt, Avantika Tiwari, Shivaji Mane, Suyodhan Reddy   +5 more
doaj   +2 more sources

Congenital absence of the penis (aphallia): A rare case report. [PDF]

Medicine (Baltimore), 2019
Abstract Rationale: Absence of the penis, known as aphallia, is a very rare congenital anomaly. It is believed to be a result of either the absence of the genital tubercle or its failure to fully develop and is associated with the level of hormones and chromosomal rearrangements.
Qiang S, Li FY, Zhou Y, Yuan Y, Li Q.
europepmc   +3 more sources

Congenital aphallia: From embryology to management - a focused minireview. [PDF]

World J Clin Pediatr
Aphallia, or penile agenesis, is an extremely rare congenital anomaly with fewer than 100 cases reported worldwide. It results from failed development of the genital tubercle during early embryogenesis, leading to complete absence of penile structures and abnormal urethral opening. This defect is often part of a broader caudal developmental disturbance
Nahid E, Ahmad MF, Shafique MA.
europepmc   +2 more sources

Tricholithobezoar: an unusual late complication of neourethral reconstruction in aphallia. [PDF]

Korean J Urol, 2013
An 18-year-old man born with aphallia had undergone phallic reconstruction in childhood followed by total urethral reconstruction with a buccal mucosal graft and groin-based pedicle (Singapore) flap urethroplasty at 13 years of age. The patient presented with obstructive voiding symptoms lasting 6 months followed by acute urinary retention. The results
Singh V, Nagathan DS, Sinha RJ, Gupta DK.   +3 more
europepmc   +4 more sources

Aphallia: do sociocultural issues affect treatment decisions? [PDF]

BMJ Case Rep, 2018
Otherwise healthy 1-month-old male patient (documented 46,XY karyotype) was referred to the plastic surgery unit for assessment. Physical exam revealed absence of penis and urethra along with a well-formed scrotum and both normally descended testicles (figure 1). No characteristic facial phenotype was noted.
Palacios-Juárez J, Hanson-Viana E, Rodríguez-Quintero JH, Morales-Maza J.   +3 more
europepmc   +4 more sources

A Case Report of Penis Agenesis (Aphallia) [PDF]

Journal of Kerman University of Medical Sciences, 2005
A neonate was admitted on the second day of birth in the pediatric ward of Kerman medical sciences university No. 1 Hospital, because of abdominal distention and the absence of penis.
B.B Bijari, P Niknafs, MH Torabinejad
doaj   +1 more source

P140: Aphallia: A complex case of a rare anomaly

Genetics in Medicine Open, 2023
Lauren Carter, Caitlin Bozick
doaj   +2 more sources