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Description: An imperforate hymen is the most commonly encountered anomaly that results from abnormalities in the development or canalization of the müllerian ducts.
Prevalence: Uncommon. Thought to be 1/5000 live-born females.
Predominant Age: Generally not diagnosed until puberty; occasionally diagnosed soon after birth (mucocolpos).
Genetics: No genetic pattern.
Causes: Failure of the endoderm of the urogenital sinus and the epithelium of the vaginal vestibule to fuse and perforate during embryonic development.
Risk Factors: None known.
Vaginal obstruction
Primary amenorrhea
Cyclic abdominal pain
Hematocolpos
Urinary retention
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