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case-report

Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy

Introduction Congenital megalourethra is typically characterized by the aplasia of penile erectile tissue, leading to abnormal dilation of the anterior urethra without structural obstruction(1,2). This terminology was first used in 1955 to describe an infant with abnormally enlarged penis and worsening renal function(2). In 1989, Benacerraf et al.(3) diagnosed megalourethra for the first time on fetal ultrasound. Congenital megalourethra is a rare condition. The prevalence is not known since

Do Duy Anh, Ha To Nguyen, Simon Meagher, Edward Araujo Júnior

Journal of Ultrasonography , ISSUE 79, 302–304

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