
doi: 10.1007/bf02722603
pmid: 11758140
Kawasaki disease (KD) is a systemic necrotizing vasculitis affecting medium and small sized arteries. The diagnosis is based entirely on recognition of a typical sequence of clinical features. Detection of any one clinical feature does not have any diagnostic significance. We report an uncommon case of Kawasaki disease in 10 months old male child with the analysis of its natural history, etiopathology, treatment and prognosis of the disease.
Male, C-Reactive Protein, Aspirin, Anti-Inflammatory Agents, Non-Steroidal, Humans, Immunoglobulins, Intravenous, Infant, Blood Sedimentation, Mucocutaneous Lymph Node Syndrome
Male, C-Reactive Protein, Aspirin, Anti-Inflammatory Agents, Non-Steroidal, Humans, Immunoglobulins, Intravenous, Infant, Blood Sedimentation, Mucocutaneous Lymph Node Syndrome
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