遗传性肾脏疾病和遗传咨询。

M R Kaplan
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引用次数: 2

摘要

遗传性肾脏异常和疾病比获得性疾病更少见。然而,他们非常感兴趣,因为他们的研究结果增加了对胚胎发生和肾脏生理学的理解,获得性疾病的发病机制,改进了治疗方法和遗传咨询的准确性。肾脏的遗传性缺陷可能是结构性的、功能性的,也可能是遗传性全身性疾病的一部分,这些疾病对肾脏结构和/或功能有重大影响。除了各种形式的囊性疾病和遗传性肾炎外,大多数肾脏的结构性缺陷都是先天性的,只有很少的情况是孟德尔遗传的。大多数遗传遗传的近端和远端肾小管功能异常是由先天代谢错误或酶缺陷和缺陷引起的。羊膜穿刺术、超声检查和酶分析使许多遗传性肾脏疾病的产前诊断成为可能,从而提供更准确的咨询和早期治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inherited renal disease and genetic counseling.

Inherited renal abnormalities and diseases are less common than acquired disorders. However, they are of great interest because their study results in increased understanding of the embryogenesis and physiology of the kidney, the pathogenesis of acquired disease, improved therapeutic approaches and accuracy of genetic counseling. Inherited defects of the kidney may be structural, functional or part of genetically transmitted systemic diseases that have major effects on renal structure and/or functions. Most structural defects of the kidney, with the exception of varying forms of cystic disease and the hereditary nephritides, are congenital and only rarely inherited in a Mendelian sense. The majority of genetically transmitted abnormalities of proximal and distal tubular function are caused by inborn metabolic errors or enzyme defects and deficiencies. Amniocentesis, ultrasonography and enzymatic assays have made the prenatal diagnosis of many inherited renal diseases possible so that more accurate counseling early therapeutic intervention may be provided.

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