肝外胆道闭锁与血清γ -谷氨酰转肽酶活性正常1例。

JPGN reports Pub Date : 2024-10-17 eCollection Date: 2024-11-01 DOI:10.1002/jpr3.12131
Benno Kohlmaier, Heidelis Tichy, Jasmin Blatterer, Holger Till, Axel Schlagenhauf, A S Knisely
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引用次数: 0

摘要

胆道闭锁婴儿血清γ -谷氨酰转肽酶(GGT)活性正常(“低”),因为GGT通常在胆道闭锁时升高。胆道闭锁低ggt胆固醇淤积的机制尚不明确,但这种现象与较差的临床结果有关。本例患者的检测显示,与预后不良和低ggt胆固醇淤积症相关的几种疾病的突变基因没有变异;事实上,在14个月大时,她的病情稳定,生物标志物值不显著。尽管如此,我们建议对此类患者进行更广泛的调查,包括基因检测,以发现共存的疾病,并扩大对胆道闭锁中GGT的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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