肾脏疾病的遗传学:罕见疾病的意外作用。

IF 15.1 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Annual review of medicine Pub Date : 2023-01-27 Epub Date: 2022-11-14 DOI:10.1146/annurev-med-042921-101813
Mark D Elliott, Hila Milo Rasouly, Ali G Gharavi
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引用次数: 0

摘要

目前已确认的慢性肾脏病遗传病因有数百种,虽然单个病因罕见,但合在一起对成人和儿童疾病都有重大影响。传统的遗传学方法在很大程度上依赖于鉴定有多个患病成员的大家族,这也是鉴定遗传性肾脏疾病的基础。随着大规模并行测序技术的广泛应用和基因型归因方法的改进,我们可以对大量无关联个体的罕见变异进行分析,从而为患者提供个性化治疗并取得重大研究进展。本综述评估了罕见疾病对患者护理和遗传性肾脏疾病研究的贡献,并重点介绍了利用新技术提高我们鉴定新基因-疾病关联能力的主要进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetics of Kidney Disease: The Unexpected Role of Rare Disorders.

Hundreds of different genetic causes of chronic kidney disease are now recognized, and while individually rare, taken together they are significant contributors to both adult and pediatric diseases. Traditional genetics approaches relied heavily on the identification of large families with multiple affected members and have been fundamental to the identification of genetic kidney diseases. With the increased utilization of massively parallel sequencing and improvements to genotype imputation, we can analyze rare variants in large cohorts of unrelated individuals, leading to personalized care for patients and significant research advancements. This review evaluates the contribution of rare disorders to patient care and the study of genetic kidney diseases and highlights key advancements that utilize new techniques to improve our ability to identify new gene-disease associations.

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来源期刊
Annual review of medicine
Annual review of medicine 医学-医学:内科
CiteScore
24.90
自引率
0.00%
发文量
58
期刊介绍: The Annual Review of Medicine, which has been published since 1950, focuses on important advancements in diverse areas of medicine. These include AIDS/HIV, cardiology, clinical pharmacology, dermatology, endocrinology/metabolism, gastroenterology, genetics, immunology, infectious disease, neurology, oncology/hematology, pediatrics, psychiatry, pulmonology, reproductive medicine, and surgery. The journal's current volume has transitioned from a gated access model to an open access model through the Annual Reviews' Subscribe to Open program. All articles published in the journal are now available under a CC BY license.
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