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Diagnosis and treatment discussion of congenital factor VII deficiency in pregnancy: A case report
BACKGROUND: Congenital factor VII deficiency (FVIID) is a rare autosomal recessive genetic disorder. The clinical manifestations of this deficiency vary greatly. Predicting the risk of bleeding during and after childbirth of pregnant women with congenital FVIID is difficult. Recombinant factor VIIa...
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| Veröffentlicht in: | World J Clin Cases |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Baishideng Publishing Group Inc
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8316952/ https://ncbi.nlm.nih.gov/pubmed/34368331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v9.i21.6091 |
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