Congenital hypofibrinogenemia

Congenital hypofibrinogenemia is a rare, inherited blood disorder characterized by the low levels of fibrinogen in the blood. Fibrinogen is a protein that plays a crucial role in blood clotting.

Pronunciation

Congenital hypofibrinogenemia is pronounced as kuhn-JEN-i-tl hye-poh-fye-brih-noh-JEE-nee-uh.

Etymology

The term "Congenital hypofibrinogenemia" is derived from the following roots:

• Congenital: From the Latin congenitus, meaning "born with".
• Hypo-: From the Greek hypo, meaning "under" or "less than normal".
• Fibrinogen: From the Latin fibrina, meaning "fibrin", and the Greek -gen, meaning "producer of".
• -emia: From the Greek haima, meaning "blood".

Symptoms

The symptoms of Congenital hypofibrinogenemia can vary greatly among individuals. Some people may experience no symptoms, while others may have mild to severe bleeding problems.

Diagnosis

Diagnosis of Congenital hypofibrinogenemia is based on the results of blood tests that measure the amount of fibrinogen in the blood.

Treatment

Treatment for Congenital hypofibrinogenemia typically involves managing symptoms and preventing complications. This may include the use of blood transfusions or fibrinogen replacement therapy.

Related Terms

• Fibrinogen
• Blood clot
• Blood transfusion
• Coagulation
• Hemostasis

See Also

• Congenital afibrinogenemia
• Dysfibrinogenemia
• Hypodysfibrinogenemia

External links

• Medical encyclopedia article on Congenital hypofibrinogenemia
• Wikipedia's article - Congenital hypofibrinogenemia

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