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“Sickle cell trait and haemophilia: a rare association”
In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associate...
Uloženo v:
| Vydáno v: | Pan Afr Med J |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The African Field Epidemiology Network
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5987143/ https://ncbi.nlm.nih.gov/pubmed/29875973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2018.29.92.14551 |
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