Hereditary protein C deficiency with portal vein thrombosis in a Chinese male: A case report

Hereditary protein C deficiency (PCD) is caused by mutation in the PC gene (PROC). The homozygous mutation form of PCD is rare. Furthermore, in Asia, cases of noncirrhotic patients with portal vein thrombosis (PVT) secondary to PCD have been rarely reported. The present study reported the case of a...

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Detalles Bibliográficos
Autores principales: Zou, Chun, Li, Tingying, Long, Liu, Liu, Liu, Zhu, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748703/
https://www.ncbi.nlm.nih.gov/pubmed/36561968
http://dx.doi.org/10.3892/etm.2022.11688

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748703/
https://www.ncbi.nlm.nih.gov/pubmed/36561968
http://dx.doi.org/10.3892/etm.2022.11688

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