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A case report of atypical autosomal dominant polycystic kidney disease presenting as glomerulocystic kidney superimposed with thin basement membrane nephropathy

Crossref DOI link: https://doi.org/10.1186/s12882-025-04170-8

Published Online: 2025-05-15

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

Authors

Wang, Wenji

Chen, Lin

Ding, Feng

Li, Xuezhu
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Text and Data Mining valid from 2025-05-15

Version of Record valid from 2025-05-15
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Article History

Received: 30 April 2024

Accepted: 8 May 2025

First Online: 15 May 2025

Declarations

:

: This study was approved by the Ethics Committee of Shanghai Ninth People’s Hospital Affiliated Shanghai Jiaotong University School of Medicine, the reference number is SH9H-2025-T129-1. The study adhered to the Declaration of Helsinki. Written informed consent were obtained from patient for ethics approval and consent to participate.

: Written informed consent were obtained from the patient and all family members for publication of this case report and any accompanying images.

: The authors declare no competing interests.

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