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An exceptional cause for the coexistence of chronic kidney disease with progressive sensorineural hearing loss: double mutations in the PKD2 and GJB2 genes

Crossref DOI link: https://doi.org/10.1186/s43162-025-00560-4

Published Online: 2025-10-30

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Kaynar, Kubra

Ertan, Hakan

Dibe, Ela

Çıkrıkçı, Özge
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Text and Data Mining valid from 2025-10-30

Version of Record valid from 2025-10-30
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Article History

Received: 4 September 2025

Accepted: 19 October 2025

First Online: 30 October 2025

Declarations

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: Written informed consent was obtained from the patient.

: The authors declare no competing interests.

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