Kumar, Mani KantNarayan, Raghvendra2026-06-022026-06-022011https://hdl.handle.net/20.500.14572/6336Mani Kant Kumar Assistant Professor, Department of Paediatrics, Narayan Medical College and Hospital, Jamuhar, Sasaram, Bihar Raghvendra Narayan Associate Professor, Department of Paediatrics, Narayan Medical College and Hospital, Jamuhar, Sasaram, BiharAbstract: Wiskott-Aldrich syndrome is an X-linked recessive disorder characterized by thrombocytopenia, eczema and recurrent infections. We report a 15 month old boy who had presented with lower gastrointestinal bleed, recurrent infections and eczema. Blood picture revealed microthrombocytopenia, high IgA and IgE, and low IgM and Normal IgG levels. A diagnosis of Wiskott-Aldrich Syndrome was made, which was missed by many paediatrician even after prolonged hospital stay before admission in our Institute. The recent progress in understanding of the pathophysiology and treatment are discussed.en-USWiskott-Aldrich syndromeEczemaMicrothrombocytopeniaWiskott Aldrich Syndrome, often Missed: A Case Report and ReviewArticle