Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare inherited disorder
characterized by progressive loss of kidney function, nonsignificant urinalysis and …

There are 3 major forms of autosomal dominant tubulointerstitial kidney disease (ADTKD):
ADTKD due to UMOD mutations, MUC1 mutations, and mutations in the REN gene …

Introduction Genetic kidney diseases are underdiagnosed; namely, from 7% to 40% of
patients suffering from chronic kidney disease (CKD) can carry a pathogenic variant …

Rationale & Objective Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a
rare underdiagnosed cause of end-stage renal disease (ESRD). ADTKD is caused by …

Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a recently defined entity
that includes rare kidney diseases characterized by tubular damage and interstitial fibrosis …

Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a clinical entity defined by
interstitial fibrosis with tubular damage, bland urinalysis and progressive kidney disease …

Autosomal dominant tubulointerstitial kidney disease (ADTKD) refers to a group of disorders
with a bland urinary sediment, slowly progressive chronic kidney disease (CKD), and …

Background Autosomal dominant tubulointerstitial kidney disease (ADTKD) caused by
mutations in the UMOD gene (ADTKD-UMOD) is considered rare and often remains …

The clinical characteristics of autosomal dominant tubulointerstitial kidney disease (ADTKD)
include bland urinary sediment, slowly progressive chronic kidney disease (CKD) with many …

Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic
cause of renal impairment resulting from mutations in the MUC1, UMOD, HNF1B, REN, and …