Haemophilia
RX Note
JULY 5, 2025
Introduction Haemophilia is a hereditary X-linked recessive bleeding disorder caused by a chromosomal mutation resulting a deficiency or absence of Coagulation factor VIII - Haemophilia A Coagulation factor IX - Haemophilia B Female carrying a FVIII or FIX gene mutation are carriers. Obligate carriers of hemophilia are daughters who inherit the mutated X chromosome from their father.
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