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MIS-C, inherited metabolic diseases and methylmalonic acidemia: a case report and review of the literature

2024-03-06

Abstract excerpt

<title>Abstract</title> <p>Bacground Methylmalonic acidemia (MMA) secondary to mutase deficiency, <italic>mut0</italic>, is an inborn error of metabolism causing complete enzyme deficiency. Multisystem Inflammatory Syndrome in Children (MIS-C) is a hyperinflammatory syndrome characterized by fever, inflammation, multiorgan impairment that manifests 14–60 days after the SARS-CoV-2 infection in patients aged < 21 y...

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Literature Corpus work
9d0b8ef0-9463-5980-8182-7222a71926dc
DOI
10.21203/rs.3.rs-3912087/v1
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MIS-C, inherited metabolic diseases and methylmalonic acidemia: a case report and review of the literatureDOI 10.21203/rs.3.rs-3912087/v1
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