Home Latest news Genetics, diagnosis and clinical features of congenital hypodysfibrinogenaemia

Genetics, diagnosis and clinical features of congenital hypodysfibrinogenaemia

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The journal Journal of Thrombosis and Haemostasis has published a report about hypodysfibrinogenaemia. Hypodysfibrinogenaemia is a rare disease characterised by decreased levels of a dysfunctional fibrinogen. It shares features with both hypo- and dysfibrinogenaemia, although with specific molecular patterns and clinical phenotypes. The full-text report you can find here.

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