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

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

Abstract Background Methylmalonic acidemia (MMA) secondary to mutase deficiency, mut0, is an inborn error of metabolism causing complete enzyme defect, allowing a high risk of irreversible complications, secondary to metabolic decompensation, induced by infections and the hyperinflammatory state. Mu...

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Bibliographic Details
Main Authors: Maria Cristina Maggio, Cinzia Castana, Marina Caserta, Antonella Di Fiore, Vittoria Siciliano, Giovanni Corsello
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Italian Journal of Pediatrics
Subjects:
MIS-C
Inherited metabolic diseases
Methylmalonic academia
Anakinra
Intravenous immunoglobulins
Online Access:https://doi.org/10.1186/s13052-025-02052-1
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