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Översättningar
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Vad betyder afibrinogenemia inom medicin ?
Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder. The lack of fibrinogen expresses itself with excessive and, at times, uncontrollable bleeding
https://en.wikipedia.org/wiki/Congenital_afibrinogenemia
Möjliga synonymer till afibrinogenemia
- afibrinogenaemia [ medicine ]