Unicornuate uterus with a rudimentary non-communicating cavitary horn in association with VACTERL association: a rare case report

单角子宫伴有不相通的原始腔角,并合并VACTERL综合征:一例罕见病例报告

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Abstract

Mullerian anomalies are malformations that affect the embryological development of paramesonephric ducts and are associated with multiple urogenital defects due to shared embryology, including VACTERL association, which coexists in about one-third of these patients. We report a rare case of a unicornuate noncommunicating horn uterus with a rudimentary second horn in a known case of VACTERL association in a 16-year-old girl.

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