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低血压的遗传学与分子生物学

Genetics and molecular biology of hypotension.

作者信息

Robertson D

机构信息

Clinical Research Center, Vanderbilt University, Nashville, TN 37232-2195.

出版信息

Curr Opin Nephrol Hypertens. 1994 Jan;3(1):13-24. doi: 10.1097/00041552-199401000-00002.

Abstract

Major strides in the molecular biology of essential hypertension are currently underway. This has tended to obscure the fact that a number of inherited disorders associated with low blood pressure exist and that these diseases may have milder and underrecognized phenotypes that contribute importantly to blood pressure variation in the general population. This review highlights some of the gene products that, if abnormal, could cause hypotension in some individuals. Diseases due to abnormalities in the catecholamine enzymes are discussed in detail. It is likely that genetic abnormalities with hypotensive phenotypes will be as interesting and diverse as those that give rise to hypertensive disorders.

摘要

目前,原发性高血压的分子生物学正在取得重大进展。这往往掩盖了这样一个事实,即存在一些与低血压相关的遗传性疾病,并且这些疾病可能具有较轻且未被充分认识的表型,这些表型对普通人群的血压变化有重要影响。本综述重点介绍了一些基因产物,如果这些基因产物异常,可能会导致某些个体出现低血压。文中详细讨论了儿茶酚胺酶异常所致的疾病。具有低血压表型的基因异常可能会像导致高血压疾病的基因异常一样有趣且多样。

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