The combination of congenital absence of the cervix and vagina is an extremely infrequent anatomic abnormality. We report a patient in whom this combination was diagnosed preoperatively by magnetic resonance imaging and managed surgically in a two-stage procedure using a modified McIndoe vaginoplasty followed by the creation of a uterovaginal fistula.
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Gerard S. Letterie (1998) studied this question.
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