在遗传代谢疾病中的心脏表现
José Ángel Cuenca-Gómez1, Carmen María Lara-Rojas2, Antonio Bonilla-López3
1Internal Medicine Service Hospital de Poniente El Ejido, Almería, Spain; Working Group on Minority Diseases of the Spanish Society of Internal Medicine (GTEM-SEMI), Almería, Spain.
遗传代谢性疾病 (IMD) 是一种影响代谢途径的罕见遗传性疾病,通常导致心肌病和心律失常等心脏问题. 本综述详细介绍了IMD的心脏表现和诊断症状.
科学领域:
- 心脏病学 心脏病学
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 遗传代谢性疾病 (IMD) 是由于遗传酶缺陷导致代谢途径阻塞的结果.
- IMDs很罕见,单独影响的不到1/100,000出生.
- 心脏表现很常见,包括心肌病变,心律失常以及膜/冠状动脉病理.
研究的目的:
- 提供IMDs与心脏参与的叙事审查.
- 描述IMDs的特定心脏表现.
- 概述有助于IMD诊断的全身症状.
主要方法:
- 对心脏表现的IMD进行文献搜索.
- 综合有关疾病特异性心脏和全身症状的信息.
- 叙事审查方法.叙事审查方法.
主要成果:
- 常见的心脏问题包括过度缩,扩张,限制性和左心室非紧缩心肌病.
- 常见的节律障碍包括AV导电缺陷,沃尔夫-帕金森-怀特综合征和心室节律失常.
- 膜和缺血冠状动脉病理也被注意到IMD后续.
结论:
- IMD经常表现为各种心脏表现.
- 在诊断IMD时,与全身症状一起识别心脏症状至关重要.
- 本综述巩固了对影响心脏的IMDs的知识.
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