Gray Platelet Syndrome

A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated with THROMBOCYTOPENIA, enlarged platelets, and prolonged bleeding time.

Also Known As:

Grey Platelet Syndrome; Platelet alpha-Granule Deficiency; Gray Platelet Syndromes; Grey Platelet Syndromes; Platelet Syndromes, Grey; Platelet alpha Granule Deficiency; Platelet alpha-Granule Deficiencies; Syndrome, Gray Platelet; Syndrome, Grey Platelet; Syndromes, Gray Platelet; alpha-Granule Deficiencies, Platelet; alpha-Granule Deficiency, Platelet

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Blood Platelet Disorders: 129
    - Gray Platelet Syndrome: 70
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inherited Blood Coagulation Disorders: 76
    - Gray Platelet Syndrome: 70

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Disease

Drug/Important Bio-Agent (IBA)