Literature DB >> 19056873

Improving the recognition of hereditary interstitial kidney disease.

Anthony J Bleyer1.   

Abstract

Autosomal dominant tubulointerstitial kidney disease is characterized by the poorly recognized inheritance of slowly progressive renal failure leading to ESRD in later life. Patients with this condition have bland urinary sediment, and renal ultrasound typically reveals normal to small kidneys, with occasional individuals having small medullary cysts. Diagnosis relies on the clinical acumen of the nephrologist. Obtaining a thorough family history and records of affected family members is especially helpful. Kidney biopsy is frequently unhelpful, whereas genetic linkage studies or mutations in the UMOD gene may identify the problem.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19056873     DOI: 10.1681/ASN.2007121330

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  3 in total

Review 1.  Diagnosis and screening of autosomal dominant polycystic kidney disease.

Authors:  York Pei; Terry Watnick
Journal:  Adv Chronic Kidney Dis       Date:  2010-03       Impact factor: 3.620

2.  Smaller caliber renal arteries are a novel feature of uromodulin-associated kidney disease.

Authors:  Aleksander Prejbisz; Lorenz Sellin; Elżbieta Szwench-Pietrasz; Magdalena Woznowski; Ilona Michałowska; Dirk Blondin; Dariusz Sajnaga; Jorg T Epplen; Mieczysław Litwin; Gabriele Dekomien; Magdalena Januszewicz; Udo Helmchen; Joanna Matuszkiewicz-Rowińska; Marcin Adamczak; Andrzej Więcek; Andrzej Januszewicz; Lars C Rump
Journal:  Kidney Int       Date:  2015-02-11       Impact factor: 10.612

Review 3.  Uric acid as one of the important factors in multifactorial disorders--facts and controversies.

Authors:  Daria Pasalic; Natalija Marinkovic; Lana Feher-Turkovic
Journal:  Biochem Med (Zagreb)       Date:  2012       Impact factor: 2.313

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.