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Дефіцит альфа-дельта гранул

ORPHA:734· ICD-10 D69.1· Alpha delta granule deficiency

Визначення(English summary)

A rare hemorrhagic disorder due to a constitutional platelet anomaly characterized by moderate to severe deficiency in both platelet alpha-granules and dense bodies, resulting in impaired platelet function and decreased aggregation responses. Patients present increased bleeding tendency with symptoms like easy bruising, or menorrhagia.

Успадкування
Autosomal dominant, Autosomal recessive