__________ is a rare autosomal recessive disorder of platelet function associated with an abnormality of membrane glycoproteins IIb and IIIa, causing decreased platelet aggregation.

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The rare autosomal recessive disorder of platelet function associated with an abnormality of membrane glycoproteins IIb and IIIa, causing decreased platelet aggregation is Glanzmann's thrombasthenia. Bernard-Soulier syndrome is a rare autosomal recessive disorder that causes a lack of platelet function due to a deficiency of the glycoprotein receptor that binds to von Willebrand factor. von Willebrand's disease is an autosomal dominant bleeding disorder caused by a deficiency in von Willebrand factor. Congenital afibrinogenemia is a rare bleeding disorder caused by a deficiency in fibrinogen.

__________ Is a Rare Autosomal Recessive Disorder of Platelet Function