Literature DB >> 33276865

Clinical and genetic spectra of kidney disease caused by REN mutations.

Céline Schaeffer1, Eric Olinger2.   

Abstract

Heterozygous mutations in REN cause autosomal dominant tubulointerstitial kidney disease (ADTKD), an increasingly recognized entity characterized by interstitial fibrosis and tubular damage. In contrast to more common forms of ADTKD, the rarity of ADTKD-REN has precluded a thorough disease characterization. Živná and colleagues take advantage of an international patient cohort to expand the genetic and clinical spectra of ADTKD-REN and to establish genotype-phenotype correlations with important implications for patient care.
Copyright © 2020 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

Entities:  

Year:  2020        PMID: 33276865     DOI: 10.1016/j.kint.2020.08.013

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  2 in total

Review 1.  Brain dysfunction in tubular and tubulointerstitial kidney diseases.

Authors:  Davide Viggiano; Annette Bruchfeld; Sol Carriazo; Antonio de Donato; Nicole Endlich; Ana Carina Ferreira; Andreja Figurek; Denis Fouque; Casper F M Franssen; Konstantinos Giannakou; Dimitrios Goumenos; Ewout J Hoorn; Dorothea Nitsch; Alberto Ortiz; Vesna Pešić; Daiva Rastenyté; Maria José Soler; Merita Rroji; Francesco Trepiccione; Robert J Unwin; Carsten A Wagner; Andrzej Wieçek; Miriam Zacchia; Carmine Zoccali; Giovambattista Capasso
Journal:  Nephrol Dial Transplant       Date:  2021-12-28       Impact factor: 5.992

Review 2.  Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians.

Authors:  Laura Nuñez-Gonzalez; Noa Carrera; Miguel A Garcia-Gonzalez
Journal:  Int J Mol Sci       Date:  2021-10-22       Impact factor: 5.923

  2 in total

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