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The authors experienced a 6-year-old female patient with Glanzmann’s Thrombathenia
and cerebral palsy. She was admitted with epistaxis, gingival bleeding and easy bruisability.
Platelets of patients showed complete absence of aggreration in response to ADP, collagen,
and epinephrine but only first aggregation to ristocetin. After platelet aggregation test,
bone marrow aspiration, and electron micrographic examination, she was proved as... |
