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Autosomal dominant thrombocytopenia with platelet secretion defect

ORPHA:466806· ICD-10 D69.4

Definition

A rare isolated constitutional thrombocytopenia characterized by reduced platelet count and defective platelet ATP secretion, resulting in increased bleeding tendency. Clinical manifestations are easy bruising, gum bleeding, menorrhagia, spontaneous epistaxis, spontaneous muscle hematoma, and potential postpartum hemorrhage, among others.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Childhood