{Reference Type}: Case Reports
{Title}: Unicornuate uterus with a rudimentary non-communicating cavitary horn in association with VACTERL association: a rare case report.
{Author}: Alsalameh BK;Eddin BGN;Jobran AWM;
{Journal}: J Surg Case Rep
{Volume}: 2024
{Issue}: 5
{Year}: 2024 May
暂无{DOI}: 10.1093/jscr/rjae268
{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.