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An Unexpected Factor to Wellens Syndrome
Factor V Leiden deficiency, the most common inherited thrombophilia, is a risk factor for venous thromboembolism in both the heterozygous and homozygous forms. An autosomal dominant genetic condition, the pattern of incomplete penetrance leads to variable manifestations of the disease. The associati...
Gorde:
| Argitaratua izan da: | Cureus |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Cureus
2021
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8051553/ https://ncbi.nlm.nih.gov/pubmed/33880316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.14489 |
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