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Significance of a Family-based Study of Hereditary Thrombosis: A Single-family Case Series of Protein C Deficiency
Thrombophilia is a serious unpredictable complication caused by gene mutations, resulting in anticoagulant deficiencies. We herein report a single-family case series of protein C (PC) deficiency. Case 1 involved a Japanese man whose PC deficiency resulted in severe systemic thrombosis. The patients...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Japanese Society of Internal Medicine
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663546/ https://www.ncbi.nlm.nih.gov/pubmed/30918183 http://dx.doi.org/10.2169/internalmedicine.2308-18 |