医学
多囊肾病
疾病
重症监护医学
肾脏疾病
常染色体显性多囊肾病
人口
肾
肾脏疾病
生物信息学
病理
内科学
生物
环境卫生
作者
Gates B. Colbert,Mohamed Elrggal,Lovy Gaur,Edgar V. Lerma
标识
DOI:10.1016/j.disamonth.2019.100887
摘要
Autosomal dominant polycystic kidney disease is a common cause of end stage kidney disease. It is a progressive and unfortunately incurable condition that can lead to significant morbidity and kidney failure. Many more patients are diagnosed with this disease without any symptoms as the population is increasingly undergoing imaging for other problems and diagnostic workup. Our understanding of the genetic variants has increased in recent years as research continues to improve. As well, therapeutic options have developed with the FDA approval of a new treatment medication, with many others underway. This review updates the clinician on the pathophysiology, clinical aspects, and therapeutic options for patients the is form of kidney disease.
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