霍尔特-奥拉姆综合征伴肺部受累--值得借鉴的算法

IF 0.9 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING

Indian Journal of Radiology and Imaging Pub Date : 2023-11-23 DOI:10.1055/s-0043-1776882

V. S. Arunachalam, J. Valakkada, A. Ayyappan

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引用次数: 0

摘要

摘要 Holt-Oram 综合征是一种罕见的先天性心血管和附属骨骼畸形。然而，只有少数病例报告 Holt-Oram 综合征累及肺部。我们报告了一例罕见的 1 岁男性儿童患者，他出现上肢畸形和呼吸困难，被诊断为肺动脉缺损和肺动脉高压，继发于房间隔缺损。

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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Holt-Oram Syndrome with Pulmonary Involvement—A Valuable Algorithm to Follow

Abstract Holt-Oram syndrome comprises a rare spectrum of congenital cardiovascular and appendicular skeletal anomalies. However, only a few cases have reported lung involvement in Holt-Oram syndrome. We reported the rare case of a 1-year-old male child patient who presented with upper limb abnormalities and respiratory distress and was diagnosed with pulmonary agenesis and pulmonary arterial hypertension secondary to an atrial septal defect.

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来源期刊

Indian Journal of Radiology and Imaging RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-

CiteScore

1.20

自引率

0.00%

发文量

115

审稿时长

45 weeks

期刊介绍： Information not localized