Resolution of proximal tubular dysfunction after liver transplantation in ATP8B1 deficiency: A case report

Angela Marino, Nathalie Godefroid, Catherine De Magnée, Xavier Stephenne · 2026

Read Resolution of proximal tubular dysfunction after liver transplantation in ATP8B1 deficiency: A case report by Angela Marino, Nathalie Godefroid, Catherine De Magnée, Xavier Stephenne (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-13659308.txt.

Description

Angela Marino and co-authors report a child case in 2026 where a kidney flaw cleared after a liver swap. The child had a rare gene ill that scars the liver and can touch many body parts. Kidney harm from it had scarce past reports.

Before the swap, the child blood tests looked fine, yet urine held too much protein, salts, and acid loss, a Fanconi-type flaw. A donor liver from a living kin was set in place of the sick one. Soon after, all the urine flaws cleared and acid pills were no longer needed. The case hints the kidney flaw rode on the liver ill and can lift.

Catalog record

CREATORAngela Marino, Nathalie Godefroid, Catherine De Magnée, Xavier Stephenne
YEAR2026
COLLECTIONPAPERS
FORMATTXT
FILE SIZE11 KB
VERSION1.0
LICENSECC BY 4.0
RIGHTSCC BY
SOURCEEurope PMC

Source: https://europepmc.org/articles/PMC13659308

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