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Congenital Afibrinogenemia (Noun)

Meaning

A rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma.

Classification

Nouns denoting natural processes.

Examples

  • Congenital afibrinogenemia is a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma.
  • People with congenital afibrinogenemia typically suffer from prolonged bleeding following injuries and spontaneous bleeding in muscles, joints, or organs.
  • Congenital afibrinogenemia is caused by mutations in the three genes that make up fibrinogen, including fibrinogen alpha chain, fibrinogen beta chain, and fibrinogen gamma chain gene.
  • In addition to frequent oral and nasal bleeding, individuals with congenital afibrinogenemia are at increased risk of intracranial hemorrhage.
  • Mild trauma frequently causes prolonged bleeding in individuals with congenital afibrinogenemia, making participating in sports extremely high-risk.

Hypernyms

  • Inherited Disorder
  • Hereditary Disease
  • Inherited Disease
  • Genetic Abnormality
  • Genetic Defect
  • Congenital Disease
  • Hereditary Condition
  • Genetic Disorder
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