一例罕见动脉迂曲综合征肺动脉球囊成形术成功

IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

Research in Cardiovascular Medicine Pub Date : 2020-04-01 DOI:10.4103/rcm.rcm_16_20

Maryam Aliramezany, A. Firouzi, M. Parsaee, Z. Khajali

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引用次数: 1

摘要

动脉扭曲综合征(ATS)是由SLC2A10基因突变引起的一种非常罕见的常染色体隐性遗传病。在这篇文章中，我们描述了一名成年ATS患者的血管成像结果，该患者表现为肺动脉高压，经过全面评估后，他是介入球囊血管成形术的候选人。我们的患者是研究中为数不多的经皮球囊血管成形术成功的患者之一。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Successful pulmonary artery balloon angioplasty in a rare case of arterial tortuosity syndrome

Arterial tortuosity syndrome (ATS) is a very rare autosomal recessive disease which results from mutations of the SLC2A10 gene. In this article, we describe the results of vascular imaging of an adult patient with ATS who was presented with pulmonary hypertension and after a complete evaluation, he was a candidate for interventional balloon angioplasty. Our patient is one of the very limited numbers of list patients in the studies for whom percutaneous balloon angioplasty performed successfully.

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来源期刊

Research in Cardiovascular Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-

自引率

0.00%

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审稿时长

17 weeks