Young girl with congenital hypo-dysfibrogenemia presenting with an acute subdural haemorrhage

Fibrinogen plays a pivotal role in the coagulation cascade. Inherited fibrinogen disorders are a heterogenous group that includes lack or reduced fibrinogen levels or a qualitative disorder of fibrinogen, dysfibrinogenemia. In fibrinogen disorders the clinical presentation is varied. Inherited dysfi...

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主要な著者: I. N. Walmsley (著者), D. T. E. Wijegunaratne (著者), S. Satheeshkumar (著者), N. Ranasinghe (著者)
フォーマット: 図書
出版事項: Sri Lanka College of Internal Medicine, 2023-02-01T00:00:00Z.
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要約:Fibrinogen plays a pivotal role in the coagulation cascade. Inherited fibrinogen disorders are a heterogenous group that includes lack or reduced fibrinogen levels or a qualitative disorder of fibrinogen, dysfibrinogenemia. In fibrinogen disorders the clinical presentation is varied. Inherited dysfibrinogenemia is associated with a higher frequency of bleeding as well as thrombosis. We present a young girl with congenital hypo-dysfibrogenemia who suffered a significant intracerebral bleed. Herein we included a brief discussion on the diagnosis of fibrin disorders.
記述事項:10.4038/ajim.v2i1.77
2827-7260