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Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center

Crossref DOI link: https://doi.org/10.1186/s13023-025-04082-8

Published Online: 2025-10-28

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

Authors

Sayed, Bayan

Alhuthil, Raghad

Saadeh, Sermin

Al-Shareef, Turki

Alhassoun, Ibrahim

Al-Sabban, Essam
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Text and Data Mining valid from 2025-10-28

Version of Record valid from 2025-10-28
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Article History

Received: 25 June 2025

Accepted: 30 September 2025

First Online: 28 October 2025

Declarations

:

: This study was conducted in line with the principles of the Declaration of Helsinki. Approval was granted by the ethics committee of the King Faisal Specialist Hospital and Research Centre (reference number: 2231334). Written consent was obtained from the parents and/or caregivers of the patients for the genetic study.

: Not applicable.

: None.

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