Laboratoire

Studies on fibrinogen abnormalities

Congenital fibrinogen abnormalities are rare orphan diseases. They are classified as quantitative abnormalities, defined by a total deficit (afibrinogenemia) or low level (hypofibrinogenemia) of circulating fibrinogen, and as qualitative abnormalities characterized by a discrepancy between the level of circulating fibrinogen measured by a functional method and the antigenic level (dysfibrinogenemia or hypodysfibrinogenemia). Laboratory diagnosis is based on conventional hemostasis testing and is usually confirmed by genetic testing.

Le corps humain héberge des milliards de bactéries et autres micro-organismes qui influencent notre état de santé. Leur prolifération dépend de leur lieu d’hébergement, leur source de nutriments, les conditions d’humidité, et de la présence ou de l’absence d’oxygène.

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