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MRKH综合征的MRI研究进展 被引量:6

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摘要 Mayer-Rokitansky-Küster-Hauser(MRKH)综合征是由于双侧苗勒氏管发育不良导致的先天性女性生殖系统畸形,子宫受累可表现为双侧始基子宫、单侧始基子宫或子宫缺失,阴道受累表现为阴道闭锁或部分闭锁,卵巢功能多正常,可合并泌尿系统、骨骼系统、听力缺陷等多系统异常改变。MRI能较好地评估MRKH综合征患者的生殖系统受累情况,且大视野冠状面扫描能显示伴随的泌尿系统及椎体异常改变,是该病辅助诊断和术前评估的重要影像学检查方法。
出处 《放射学实践》 北大核心 2017年第1期82-85,共4页 Radiologic Practice
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