afibrinogenemia

[ey-fahy-bruh-noh-juh-nee-mee-uh]

afibrinogenemia Definition

a rare genetic disorder characterized by the absence or severe deficiency of fibrinogen, a protein that is essential for blood clotting.

Using afibrinogenemia: Examples

Take a moment to familiarize yourself with how "afibrinogenemia" can be used in various situations through the following examples!

  • Example

    Patients with afibrinogenemia are at risk of excessive bleeding and bruising.

  • Example

    The condition is usually diagnosed in childhood and requires lifelong treatment.

  • Example

    Afibrinogenemia can be inherited in an autosomal recessive pattern.

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Summary: afibrinogenemia in Brief

'Afibrinogenemia' [ey-fahy-bruh-noh-juh-nee-mee-uh] is a rare genetic disorder characterized by the absence or severe deficiency of fibrinogen, a protein that is essential for blood clotting. Patients with this condition are at risk of excessive bleeding and bruising, and it is usually diagnosed in childhood and requires lifelong treatment.