What is another word for Congenital Afibrinogenemia?
Pronunciation: [kənd͡ʒˈɛnɪtə͡l ɐfˌɪbɹɪnə͡ʊd͡ʒnˈiːmi͡ə] (IPA) 
Congenital afibrinogenemia is a rare bleeding disorder that is characterized by the absence or deficiency of fibrinogen, a protein that is essential for blood clotting. There are several synonyms for this condition, including hypofibrinogenemia, dysfibrinogenemia, fibrinogen deficiency, and factor I deficiency. Other less common synonyms include afibrinogenemia with renal disease, afibrinogenemia with pregnancy loss, and hereditary hypofibrinogenemia. While the names may differ, the underlying condition remains the same, with individuals affected by this disorder experiencing a higher risk of bleeding and related complications. Early diagnosis and prompt treatment are necessary to manage this condition effectively.
