congenital afibrinogenemia (Meaning)
congenital afibrinogenemia (n)
a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma
Synonyms & Antonyms of congenital afibrinogenemia
No Synonyms and anytonyms found
congenital afibrinogenemia Sentence Examples
- Congenital afibrinogenemia is a rare genetic disorder characterized by a complete absence of fibrinogen in the blood.
- Individuals with congenital afibrinogenemia are at increased risk of bleeding episodes, including spontaneous bleeding into joints and muscles.
- The diagnosis of congenital afibrinogenemia is typically made based on laboratory tests that confirm the absence of fibrinogen in the blood.
- Treatment for congenital afibrinogenemia often involves replacement therapy with fibrinogen concentrates to prevent or manage bleeding episodes.
- People with congenital afibrinogenemia may need to undergo regular monitoring of their clotting function and receive prophylactic treatment to prevent bleeding complications.
- Congenital afibrinogenemia is an inherited condition caused by mutations in the genes responsible for producing fibrinogen.
- The symptoms of congenital afibrinogenemia can vary widely among affected individuals, ranging from mild to severe bleeding tendencies.
- In severe cases of congenital afibrinogenemia, bleeding episodes may be life-threatening and require immediate medical intervention.
- Genetic counseling may be recommended for individuals with congenital afibrinogenemia and their families to discuss the inheritance pattern and the risk of passing the condition to future generations.
- Despite the challenges associated with congenital afibrinogenemia, many individuals with the condition lead fulfilling lives with appropriate medical management and support.
FAQs About the word congenital afibrinogenemia
a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma
No synonyms found.
No antonyms found.
Congenital afibrinogenemia is a rare genetic disorder characterized by a complete absence of fibrinogen in the blood.
Individuals with congenital afibrinogenemia are at increased risk of bleeding episodes, including spontaneous bleeding into joints and muscles.
The diagnosis of congenital afibrinogenemia is typically made based on laboratory tests that confirm the absence of fibrinogen in the blood.
Treatment for congenital afibrinogenemia often involves replacement therapy with fibrinogen concentrates to prevent or manage bleeding episodes.
