Case Report: The JAK-Inhibitor Ruxolitinib Use in Aicardi-Goutieres Syndrome Due to ADAR1 Mutation
Type I Interferonopathies comprise inherited inflammatory diseases associated with perturbation of the type I IFN response. Use of Janus kinase (JAK) inhibitors has been recently reported as possible tools for treating some of those rare diseases. We describe herein the clinical picture and treatmen...
Saved in:
Main Authors: | Marco Cattalini (Author), Jessica Galli (Author), Fiammetta Zunica (Author), Rosalba Monica Ferraro (Author), Marialuisa Carpanelli (Author), Simona Orcesi (Author), Giovanni Palumbo (Author), Lorenzo Pinelli (Author), Silvia Giliani (Author), Elisa Fazzi (Author), Raffaele Badolato (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2021-10-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Aicardi-Goutieres Syndrome
by: J Gordon Millichap
Published: (1999) -
Interferon Biomarkers in Aicardi-Goutieres Syndrome
by: J Gordon Millichap, et al.
Published: (2014) -
MRI Features Predictive of Aicardi-Goutieres Syndrome
by: J Gordon Millichap
Published: (2015) -
Heterozygous Mutation in Adenosine Deaminase Gene in a Patient With Severe Lymphopenia Following Corticosteroid Treatment of Autoimmune Hemolytic Anemia
by: Serena I. Tripodi, et al.
Published: (2018) -
Neurophenotype and genetic analysis of children with Aicardi‐Goutières syndrome in China
by: Shen Zhang, et al.
Published: (2024)