Abnormal urethral pathways in a child presenting with diphallia
نویسندگان
چکیده
Diphallia is an extremely rare embryological anomaly, occurring once in 5–6 million births. Here we discuss a neonate who was referred for surgical consultation of diphallia, which examination revealed dominant right phallus and apparently shorter left phallus. MRI retrograde urethrogram unique pathway the urethra stenosed, but otherwise normal urethra. The decision made to excise associated due correct anatomy corresponding
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ژورنال
عنوان ژورنال: Journal of pediatric surgery case reports
سال: 2021
ISSN: ['2213-5766']
DOI: https://doi.org/10.1016/j.epsc.2021.101802