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Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10376630" target="_blank" >RIV/00216208:11110/18:10376630 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1053/j.ajkd.2017.08.024" target="_blank" >https://doi.org/10.1053/j.ajkd.2017.08.024</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1053/j.ajkd.2017.08.024" target="_blank" >10.1053/j.ajkd.2017.08.024</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation

  • Original language description

    Mucin 1 kidney disease, previously referred to as medullary cystic kidney disease type 1, is a rare hereditary kidney disease. It is one of several diseases now termed autosomal dominant tubulointerstitial kidney disease, as proposed by a KDIGO (Kidney Disease: Improving Global Outcomes) consensus report in 2014. Autosomal dominant tubulointerstitial kidney diseases share common clinical findings, such as autosomal dominant inheritance, bland urinary sediment, absent to mild proteinuria, and progressive loss of kidney function. Although the pathophysiology of mucin 1 kidney disease is still under investigation, genetic testing has been developed to detect the most well-known mutation, a single cytosine insertion into a string of 7 cytosines in the variable-number tandem repeat (VNTR) region of the MUC-1 gene. With this diagnostic tool, nephrologists can offer genetic counseling to affected families and monitor closely for progression of disease. We report a Hispanic patient with a strong family history of chronic kidney disease who tested positive for the MUC1 mutation.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10600 - Biological sciences

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    American Journal of Kidney Diseases

  • ISSN

    0272-6386

  • e-ISSN

  • Volume of the periodical

    71

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    495-500

  • UT code for WoS article

    000428167100012

  • EID of the result in the Scopus database

    2-s2.0-85036626294