Work

[Analysis of the etiology and clinical indicators of infantile cholestasis].

Year: 2024

Type: other

Abstract: Infantile cholestasis etiology is diverse. ALP, bile acids, GGT, DBil, and albumin levels can serve as simple indicators for early-stage differentiation between inherited metabolic liver disease and biliary atresia. The cholestasis etiology should be determined as early as possible following biliary atresia exclusion by actively completing genetic metabolic gene detection.

Source: PubMed

DOI: 10.3760/cma.j.cn501113-20230905-00091

Authors: Q Z Li, C Fan, X S Zhao, Q J Liu, D Qin, P Wang, L Zhu

Language: English

Topic: Pediatric Hepatobiliary Diseases and Treatments

Subfield: Surgery

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W4403240356

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