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Glanzmann thrombasthenia

Glanzmann thrombasthenia is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation. This disease is caused by mutation in the integrin family receptor genes encoding platelet glycoprotein alpha-IIb or platelet glycoprotein IIIa.

Drugs that treat Glanzmann thrombasthenia

NovoSeven

Made by

Novo Nordisk

Approval date

2000/3/10