Myelin oligodendrocyte glycoprotein antibody-associated disease as a novel presentation of central nervous system autoimmunity in a pediatric patient with Wiskott-Aldrich syndrome

BACKGROUND: Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency caused by mutations in the WAS gene that leads to increased susceptibility to infections, thrombocytopenia, eczema, malignancies, and autoimmunity. Central nervous system (CNS) autoimmune manifestations are uncommon....

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Detalles Bibliográficos
Autores principales: Xie, Vivien X., File, Wilson, Wiedl, Christina, Ward, Brant R., Saldaña, Blachy Dávila, Keller, Michael D., Kornbluh, Alexandra B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408201/
https://www.ncbi.nlm.nih.gov/pubmed/37550789
http://dx.doi.org/10.1186/s13223-023-00827-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408201/
https://www.ncbi.nlm.nih.gov/pubmed/37550789
http://dx.doi.org/10.1186/s13223-023-00827-x

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