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Farber's Lipogranulomatosis: Multimodal Therapy With Tocilizumab and Consolidative HSCT Improves Assessment, and Long‐Term Outcome

ABSTRACT Farber's lipogranulomatosis (FL) is an autosomal recessive lipid storage disorder, arising as a consequence of genetic acid ceramidase deficiency. Clinically, it presents as severe arthritis, voice hoarseness, and widespread, painful subcutaneous nodules (SCN). For those without CNS involve...

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Bibliografische gegevens
Hoofdauteurs: Nathanael C. C. Lucas, Claire Horgan, Omima Mustafa, Srividhya Senthil, Denise Bonney, Ramya Nataraj, Sophie Fisher, Chern Tan, Stewart Rust, Simon A. Jones, Sarah Hulley, Robert Wynn
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Wiley 2025-09-01
Reeks:JIMD Reports
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Online toegang:https://doi.org/10.1002/jmd2.70041
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