Case Report: Wiskott – Aldrich Syndrome in Patients with Normal Platelet Size in Bahrain

Regardless of ethnicity or geographical distribution, Wiskott-Aldrich syndrome affects 1 in every 100,000 live male births. It has been established that may potentially be a source autoimmune illnesses and reticuloendothelial malignancies, even though most patients present with the traditional triad thrombocytopenia, eczema, recurrent bacterial infections. This case report introduces 4-year-old boy born hematemesis, recurring infections, and, surprisingly, normal platelet size. Genetic testing confirmed diagnosis, primarily based on clinical suspicion. Thus study attempts to increase awareness among doctors Bahrain globally considering diagnosis any patient infections thrombocytopenia regardless having mean volume .