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Management of dysfibrinogenemia in pregnancy: A case report
BACKGROUND: Dysfibrinogenemia is a rare coagulation disorder caused by mutations in the fibrinogen gene that results in abnormal fibrinogen function. Dysfibrinogenemia has a wide spectrum of clinical manifestations including asymptomatic(55%), hemorrhage (25%), and thrombosis (20%). METHODS: We repo...
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| Publicado no: | J Clin Lab Anal |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6816852/ https://ncbi.nlm.nih.gov/pubmed/28948631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.22319 |
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