Definición:
Group of hemorrhagic disorders in which the is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Sinónimos:
Angiohemofilia /
Enfermedad de von Willebrand /
Hemofilia Vascular /
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