Congenital Afibrinogenemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Congenital Afibrinogenemia, or a subtype of Congenital Afibrinogenemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Congenital Afibrinogenemia: Introduction
Prognosis of Congenital Afibrinogenemia: some survive to adulthood
Complications of Congenital Afibrinogenemia:
see complications of Congenital Afibrinogenemia
Symptoms of Congenital Afibrinogenemia: see symptoms of Congenital Afibrinogenemia
Complications of Congenital Afibrinogenemia: see complications of Congenital Afibrinogenemia
Onset of Congenital Afibrinogenemia: birth
Diagnostic testing: see tests for Congenital Afibrinogenemia.
Misdiagnosis: see misdiagnosis and Congenital Afibrinogenemia.
Treatments for Congenital Afibrinogenemia:
see treatments for Congenital Afibrinogenemia
Research for Congenital Afibrinogenemia:
see research for Congenital Afibrinogenemia
Main name of condition: Congenital Afibrinogenemia
Other names or spellings for Congenital Afibrinogenemia:Rabe Salmon syndrome, fibrinogenopenia congenital, Afibrinogenemia
Congenital afibrinogenaemia, Afibrinogenemia, Afibrinogenemia, congenital
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, Congenital Afibrinogenemia:
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