Article

The first reported case of Noonan syndrome complicated with hepatocellular carcinoma.

2021-03-20

Abstract excerpt

Noonan syndrome is a genetic multisystem disorder characterized by distinctive facial features, developmental delay, congenital heart disease, and other conditions. It is associated with mutation of genes encoding the proteins in the RAS-MAPK pathway, including PTPN11. We herein describe the first case of Noonan syndrome complicated with hepatocellular carcinoma.

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Literature Corpus work: 10769df8-c644-56ac-a2ac-ad5608b0861a
DOI: 10.22541/au.161625972.22522023/v1

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