Á lódáil...
Afibrinogénémie congénitale: à propos d’une observation
Afibrinogenemia is a rare dyscrasia characterized by a congenital fibrinogen deficiency It is transmitted in an autosomal recessive manner. Hemorrhagic manifestations are variable and can be life-threatening. A little more than 250 cases have been published up till now. We here report a new case of...
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| Foilsithe in: | Pan Afr Med J |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
The African Field Epidemiology Network
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5337292/ https://ncbi.nlm.nih.gov/pubmed/28293349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2016.25.233.10754 |
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