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Published in 2023 at "Journal of inherited metabolic disease"
DOI: 10.1002/jimd.12592
Abstract: OBJECTIVES Mutations in the LPIN1 gene constitute a major cause of severe rhabdomyolysis (RM). The TLR9 activation prompted us to treat patients with corticosteroids in acute conditions. METHODS In patients with LPIN1 mutations, RM and…
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Keywords:
rhabdomyolysis;
systemic corticosteroids;
corticosteroid treated;
treated corticosteroids ... See more keywords