소아에서 일측 무신증 및 골반강 내 낭종성 종물을 동반한 Mayer-Rokitansky-Kuster-Hauser 증후군

Abstract

The Mayer-Rokitansky-Kuster-Hauser syndrome represents a spectrum of mullerian anomalies, including vaginal agenesis with or without renal anomalies, in genotypically and phenotypically normal female subjects with normal endocrine status. We experienced a case of this anomaly which combined with unilateral renal agenesis and pelvic cystic mass in child.