Wiskott-Aldrich syndrome
ORPHA:906· ICD-10 D82.0
Definition
A primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.
- Prevalence
- 1-9 / 1 000 000
- Inheritance
- Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive
- Age of onset
- Infancy, Neonatal