Genetic testing for kidney disease of unknown etiology

被引:39
|
作者
Hays, Thomas [1 ]
Groopman, Emily E. [2 ]
Gharavi, Ali G. [2 ,3 ,4 ]
机构
[1] Columbia Univ, Dept Pediat, Div Neonatol & Perinatol, Vagelos Coll Phys & Surg, New York, NY USA
[2] Columbia Univ, Dept Med, Div Nephrol, Vagelos Coll Phys & Surg, New York, NY USA
[3] Columbia Univ, Inst Genom Med, Vagelos Coll Phys & Surg, New York, NY USA
[4] Columbia Univ, Ctr Precis Med & Genom, Dept Med, Vagelos Coll Phys & Surg, New York, NY USA
基金
美国国家卫生研究院;
关键词
chronic kidney disease; genetic testing; kidney disease of unknown etiology; 22Q11.2 DELETION SYNDROME; DE-NOVO MUTATIONS; STEROID-RESISTANT; CLINICAL EXOME; CONGENITAL-ANOMALIES; GENOMIC DISORDERS; MEDICAL GENETICS; AMERICAN-COLLEGE; VARIANTS; RARE;
D O I
10.1016/j.kint.2020.03.031
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
In many cases of chronic kidney disease, the cause of disease remains unknown despite a thorough nephrologic workup. Genetic testing has revolutionized many areas of medicine and promises to empower diagnosis and targeted management of such cases of kidney disease of unknown etiology. Recent studies using genetic testing have demonstrated that Mendelian etiologies account for approximately 20% of cases of kidney disease of unknown etiology. Although genetic testing has significant benefits, including tailoring of therapy, informing targeted workup, detecting extrarenal disease, counseling patients and families, and redirecting care, it also has important limitations and risks that must be considered.
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页码:590 / 600
页数:11
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