粘多糖病I-S型合并主动脉瓣和二尖瓣狭窄1例报道。

Q4 Medicine

Journal of Tehran University Heart Center Pub Date : 2021-01-01 DOI:10.18502/jthc.v16i1.6598

Hakimeh Sadeghian, Afsaneh Sadeghian, Bahareh Eslami, Seyed Hesameddin Abbasi, Masoumeh Lotfi-Tokaldany

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引用次数: 2

摘要

粘多糖病(MPS)综合征是一种遗传性代谢紊乱。在超过一半的MPS综合征患者中，有心脏瓣膜受累的报道;然而，MPS综合征I-S型合并主动脉瓣和二尖瓣狭窄是非常罕见的。我们描述了一个39岁的男性严重二尖瓣和主动脉瓣狭窄由于MPS综合征I-S型。经胸和经食管超声心动图显示主动脉瓣和二尖瓣严重增厚和钙化，伴有严重的左心室肥厚。冠状动脉造影显示正常。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Combined Aortic and Mitral Valve Stenosis in Mucopolysaccharidosis Syndrome Type I-S: A Report of a Rare Case.

查看原文本刊更多论文

Combined Aortic and Mitral Valve Stenosis in Mucopolysaccharidosis Syndrome Type I-S: A Report of a Rare Case.

Mucopolysaccharidosis (MPS) syndrome is an inherited metabolic disorder. In more than half of the patients with MPS syndrome, heart valve involvement is reported; however, combined aortic and mitral valve stenosis in MPS syndrome type I-S is very rare. We describe a 39-year-old man with severe mitral and aortic valve stenosis due to MPS syndrome type I-S. Transthoracic and transesophageal echocardiography revealed severe thickening and calcification in the aortic and mitral valves with severe left ventricular hypertrophy. The coronary arteries were normal in angiography.

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来源期刊

Journal of Tehran University Heart Center Medicine-Cardiology and Cardiovascular Medicine

CiteScore

0.90

自引率

0.00%

发文量

审稿时长

12 weeks