Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency

INTRODUCTION: LPIN1 deficiency is an autosomal recessive form of early childhood recurrent severe rhabdomyolysis. Although not completely lucid yet, LPIN1 has been shown to modulate endosomal-related pro-inflammatory responses via peroxisome proliferator-activated receptor α (PPARα) and PPARγ coacti...

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Detalles Bibliográficos
Autores principales: Yeganeh, Mehdi, March, Kaitlin, Jones, Catherine, Ho, Gloria, Selby, Kathryn A., Chanoine, Jean-Pierre, Stockler, Sylvia, Salvarinova, Ramona, Horvath, Gabriella, Brunel-Guitton, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024045/
https://www.ncbi.nlm.nih.gov/pubmed/36941958
http://dx.doi.org/10.1016/j.ymgmr.2023.100961

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024045/
https://www.ncbi.nlm.nih.gov/pubmed/36941958
http://dx.doi.org/10.1016/j.ymgmr.2023.100961

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