Severe autosomal recessive macrothrombocytopenia

Orpha code: 438207OMIM code: 616176

Definition

A rare isolated hereditary giant platelet disorder characterized by severe thrombocytopenia and thrombopathy due to defects in proplatelet formation and platelet activation in homozygous patients. Clinical manifestation are recurrent bleeding episodes including epistaxis, spontaneous hematomas, and menorrhagia.

Disease data
Classification

Disease

ORPHA code
438207
OMIM code
616176
ICD10 code
D69.4
ICD11 code
-

No additional description.

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