Results 81 to 90 of about 232 (115)
An update on penile reconstruction. [PDF]
Asian J Androl, 2011 Garaffa G, Raheem AA, Ralph DJ.
europepmc +1 more source
Updates on the Care of Cloacal Exstrophy. [PDF]
Children (Basel)Ostertag-Hill CA +3 more
europepmc +1 more source
Rectourethral Fistula after Posterior Urethral Valves Ablation in an Infant: A Rare Complication.
J Indian Assoc Pediatr SurgBhardwaj A +3 more
europepmc +1 more source
Management of andrological disorders from childhood and adolescence to transition age: guidelines from the Italian Society of Andrology and Sexual Medicine (SIAMS) in collaboration with the Italian Society for Pediatric Endocrinology and Diabetology (SIEDP) - part-2. [PDF]
J Endocrinol InvestBonomi M +10 more
europepmc +1 more source
Aphallia: a review to standardize management
Pediatric Surgery International, 2018 Congenital aphallia is a rare anomaly with little supporting literature and controversial management. The aim of this review is to assess the most recent literature with a focus on staged management of these cases. We performed a PubMed search of all English literature in the past 10 years using the term aphallia.
Tarryn Gabler, Jerome Loveland
exaly +4 more sources
Aphallia in an adult male with 46,XY karyotype
International Journal of Urology, 2011 AbstractAphallia is a rare urogenital anomaly with an estimated incidence of 1 in 10–30 million. We report a case of aphallia in a male, who had two well‐developed testicles, but lacked a penis. Digital rectal examination revealed the urethral meatus was opening to the anterior wall of the rectum posterior to the sphincter.
Kaimin Guo, Fubiao Li
exaly +4 more sources
Male Gender Assignment in Aphallia: A Case Report and Review of the Literature
International Urology and Nephrology, 2005 Aphallia is known to be a very rare congenital malformation, with an occurrence of 1 in every 30 million births; only 75 cases have been reported in the literature till recently (Hendren WH. J Urol 1997; 157: 1469-1474). Gender reassingnment is recommended for the affected newborns in infancy (Elder JS. In: Walsh PC, Retik AB, eds.
Hemendra N. Shah, Pritesh Jain
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Aphallia, Lung Agenesis and Multiple Defects of Blastogenesis
Fetal and Pediatric Pathology, 2011 We report the association of aphallia, with imperforate anus, bilateral renal dysplasia and complete right lung agenesis in a fetus born of non-consanguineous parents. No maternal diabetes was present. The multiple mesodermal anomalies present in this male fetus, with a severe form of Uro-Rectal-Septum Malformation Sequence associated with unilateral ...
Sandrine Passemard +2 more
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