Abstract
AbstractA 2-month-old newborn was hospitalized for hemorrhagic picture associated with deterioration of his general condition and eczema. A thrombocytopenia is highlighted, without any other alteration of coagulation. As the patient develops pneumocystis jirovecii infection and signs of vasculitis, immune deficiency is suspected. The discovery of CD8 lymphopenia, microthrombocytopenia, and the presence of eczema, lead to a diagnosis of Wiskott-Aldrich syndrome, then confirmed by molecular biology.
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