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Laboratory findings included elevated serum amyloid-A, erythrocyte sedimentation rate, and complete proteins in urine tests. Perfect blood count showed mild microcytic hypochromic anemia. The molecular evaluation had been imperative to confirm the provisional clinical analysis. H syndrome is a rare autoinflammatory syndrome with pleiotropic manifestations that impact many organs and may be mistaken for other problems. Our person's description may increase the phenotype of H syndrom
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