Extrahepatic biliary atresia and normal‐range serum gamma‐glutamyltranspeptidase activity: A case report

An infant with biliary atresia had normal-range ('low') serum gamma-glutamyltranspeptidase (GGT) activity, exceptional because GGT generally is elevated in biliary atresia. Mechanisms underlying low-GGT cholestasis in biliary atresia are not defined, but the phenomenon is associated with worse clinical outcome. Testing in our patient revealed no variants in genes mutated in several disorders also associated with poor prognosis and with low-GGT cholestasis; indeed, at age 14 months she has stable disease with unremarkable biomarker values. Nonetheless, we recommend extended investigations in such patients, including genetic testing, to detect coexistent disorders and to expand understanding of GGT in biliary atresia.

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Publication Details

Journal
JPGN Reports
Published
2024-10-17
DOI
https://doi.org/10.1002/jpr3.12131
Primary Topic
Pediatric Hepatobiliary Diseases and Treatments
Type
article
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article

Extrahepatic biliary atresia and normal‐range serum gamma‐glutamyltranspeptidase activity: A case report

Jasmin Blatterer, Benno Kohlmaier, Holger Till, Alexander S. Knisely et al.
JPGN Reports
Pediatric Hepatobiliary Diseases and Treatments
article

Extrahepatic biliary atresia and normal‐range serum gamma‐glutamyltranspeptidase activity: A case report

Jasmin Blatterer, Benno Kohlmaier, Holger Till, Alexander S. Knisely, Axel Schlagenhauf, Heidelis Tichy
article en

Abstract

An infant with biliary atresia had normal-range ('low') serum gamma-glutamyltranspeptidase (GGT) activity, exceptional because GGT generally is elevated in biliary atresia. Mechanisms underlying low-GGT cholestasis in biliary atresia are not defined, but the phenomenon is associated with worse clinical outcome. Testing in our patient revealed no variants in genes mutated in several disorders also associated with poor prognosis and with low-GGT cholestasis; indeed, at age 14 months she has stable disease with unremarkable biomarker values. Nonetheless, we recommend extended investigations in such patients, including genetic testing, to detect coexistent disorders and to expand understanding of GGT in biliary atresia.

JPGN ReportsVol. 5(4)
Medical University of Graz (AT)
No poverty
Openalex Percentile: Top 66%
Pediatric Hepatobiliary Diseases and Treatments
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