Hereditary antithrombin III deficiency

Hereditary antithrombin III deficiency is an autosomal dominant hereditary disease, with equal chances for men and women. Heterozygotes are more common and there are no clinical symptoms. Only 4% of patients with venous thrombosis are ATⅢ deficiency.

The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.

Was this article helpful? Thanks for the feedback. Thanks for the feedback.