کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8774777 1599206 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Revisión de la nefropatía tubulointersticial autosómica dominante
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی بیماری‌های کلیوی
پیش نمایش صفحه اول مقاله
Revisión de la nefropatía tubulointersticial autosómica dominante
چکیده انگلیسی
In recent years there has been a reclassification of hereditary tubulointerstitial renal diseases. The old concepts of nephronoptisis or medullary cystic disease have been reordered based on the discovery of new genes. The 2015 KDIGO guidelines proposed a unification of terminology, diagnostic criteria and monitoring. So far 4 genes causing autosomal dominant tubulointerstitial kidney disease have been described: MUC1, UMOD, HNF1B and REN. Although the mutation in each of them causes distinctive features in how they present, all have in common the progressive tubulointerstitial damage and renal fibrosis. In this article, we present a review of the guidelines and the literature, and some practical recommendations for dealing with this disease.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Nefrología - Volume 37, Issue 3, May–June 2017, Pages 235-243
نویسندگان
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