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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| Main Authors: | , |
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| Format: | Book |
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Elsevier,
2017-10-01T00:00:00Z.
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