Hemophilia A carrier female newborn with novel p.M2274T mutation presented with psoas hematoma

Hemophilia A is an X-linked recessive disorder characterized by congenital deficiency of factor VIII. Mostly, males are affected. Cases of hemophilia A are unusual in females but can result from certain genetic mechanisms. The severity of bleeding in hemophilia is generally correlated with the coagu...

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Bibliographic Details
Main Authors: Baris Malbora (Author), Ozgur Kirbiyik (Author)
Format: Book
Published: Elsevier, 2017-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available