Genetic testing in chronic kidney disease of uneXplained cause (CKDx): clinical insights and evolving diagnostic paradigms

Chronic kidney disease (CKD) represents a significant global health burden, with diverse etiologies and often complex clinical presentations. Among these, a notable subset of CKD patients present without a clear underlying cause despite extensive diagnostic evaluation. For this subgroup, the term CK...

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Bibliographic Details
Main Authors: Halbritter, Jan Peter (Author) , Simons, Matias (Author)
Format: Article (Journal)
Language:English
Published: 18. Februar 2026
In: Medizinische Genetik
Year: 2026, Volume: 38, Issue: 1, Pages: 21-28
ISSN:1863-5490
DOI:10.1515/medgen-2025-2046
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1515/medgen-2025-2046
Verlag, kostenfrei, Volltext: https://www.degruyterbrill.com/document/doi/10.1515/medgen-2025-2046/html
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Author Notes:Jan Halbritter, Matias Simons
Description
Summary:Chronic kidney disease (CKD) represents a significant global health burden, with diverse etiologies and often complex clinical presentations. Among these, a notable subset of CKD patients present without a clear underlying cause despite extensive diagnostic evaluation. For this subgroup, the term CKDx - chronic kidney disease of unexplained cause, has recently been proposed. A major element of the diagnostic workup of CKDx is genetic testing, for which the methodology has greatly improved in the last years.
Item Description:Veröffentlicht: 18. Februar 2026
Gesehen am 22.04.2026
Physical Description:Online Resource
ISSN:1863-5490
DOI:10.1515/medgen-2025-2046