在阻塞性和非阻塞性多变性心肌病症病例中,附属中枢组织
İrem Türkmen1, Arda Güler1, Sezgin Atmaca1
1Department of Cardiology, University of Health Sciences, Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkiye.
概括
附属心关组织 (AMVT) 是一种罕见的先天性心脏异常. 它的成年人诊断与高伤心肌病 (HCM) 一起是非常罕见的,复杂的诊断和需要先进的成像.
科学领域:
- 心脏病学 心脏病学
- 遗传性心脏病是一种先天性心脏病.
- 心脏成像 - - 心脏成像
背景情况:
- 附属心关组织 (AMVT) 是一种罕见的先天性心脏异常.
- 它通常在儿童时期被诊断出来,成人呈现非常罕见.
- 与多变性心肌病 (HCM) 的共存特别不常见.
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