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早发性冠状动脉疾病与普拉德-威利综合征

Premature coronary artery disease and the Prader-Willi syndrome.

作者信息

Page S R, Nussey S S, Haywood G A, Jenkins J S

机构信息

Department of Medicine, St George's Hospital Medical School, London, UK.

出版信息

Postgrad Med J. 1990 Mar;66(773):232-4. doi: 10.1136/pgmj.66.773.232.

DOI:10.1136/pgmj.66.773.232
PMID:2362894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2429450/
Abstract

A 28 year old woman with the Prader-Willi syndrome developed chest pain and loss of anterior R wave amplitude on the electrocardiogram. Cardiac catheterization demonstrated a severe proximal stenosis of the left anterior descending artery with delayed antegrade flow together with antero-apical akinesia consistent with myocardial infarction. Physicians involved in the management of patients with the Prader-Willi syndrome should be aware of this association with premature coronary artery disease.

摘要

一名患有普拉德-威利综合征的28岁女性出现胸痛,心电图显示前壁R波振幅降低。心脏导管检查显示左前降支严重近端狭窄,顺行血流延迟,伴有前壁心尖运动减弱,符合心肌梗死表现。参与普拉德-威利综合征患者管理的医生应注意到这种与早发性冠状动脉疾病的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6515/2429450/a118c51205cb/postmedj00159-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6515/2429450/a118c51205cb/postmedj00159-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6515/2429450/a118c51205cb/postmedj00159-0074-a.jpg

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本文引用的文献

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.15号染色体缺失是普拉德-威利综合征的病因。
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Prader-Willi Syndrome after age 15 years.15岁之后的普拉德-威利综合征。
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'A one-sided affair': unilateral pulmonary oedema and the role of cardiac MRI in diagnosing premature coronary artery disease in a patient with Prader-Willi syndrome.“单方面的情况”:单侧肺水肿以及心脏磁共振成像在诊断普拉德-威利综合征患者冠状动脉疾病中的作用
BMJ Case Rep. 2013 May 22;2013:bcr2013008692. doi: 10.1136/bcr-2013-008692.
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C-reactive protein levels in subjects with Prader-Willi syndrome and obesity.普拉德-威利综合征和肥胖症患者的C反应蛋白水平。
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The Prader-Willi syndrome: a study of 40 patients and a review of the literature.普拉德-威利综合征:40例患者的研究及文献综述
Medicine (Baltimore). 1983 Mar;62(2):59-80.
6
Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence.普拉德-威利综合征。32例病例总结,包括一对患病的堂兄妹,其中一人身材和智力正常。
J Pediatr. 1972 Aug;81(2):286-93. doi: 10.1016/s0022-3476(72)80297-x.
7
Acanthosis nigricans in association with various genodermatoses. With emphasis on lipodystrophic diabetes and Prader-Willi syndrome.黑棘皮病与多种遗传性皮肤病相关。重点关注脂肪营养不良性糖尿病和普拉德-威利综合征。
Acta Derm Venereol. 1968;48(5):465-73.
8
A rapid banding technique for human chromosomes.一种用于人类染色体的快速显带技术。
Lancet. 1971 Oct 30;2(7731):971-2. doi: 10.1016/s0140-6736(71)90287-x.
9
Premature coronary artery atherosclerosis in a patient with Prader-Willi syndrome.一名普拉德-威利综合征患者的冠状动脉粥样硬化过早出现。
Am J Med Genet. 1987 Dec;28(4):873-80. doi: 10.1002/ajmg.1320280412.
10
Menopause and risk of cardiovascular disease: the Framingham study.更年期与心血管疾病风险:弗明汉姆研究
Ann Intern Med. 1976 Oct;85(4):447-52. doi: 10.7326/0003-4819-85-4-447.