[Type I interferonopathies. Literature review].

Abstract excerpt

Thanks to the tremendous progress of genetics, a new field of inherited inflammatory disorders related to an overproduction of interferon has recently emerged. The so-called type I interferonopathies represent an heterogeneous group of Mendelian diseases presenting with various features starting in childhood, although the diagnosis can also be made later in life. Several clinical and biological characteristics...

Topics

• Autoimmune Diseases
• Humans
• Interferon Type I
• Molecular Targeted Therapy
• Mutation
• Receptors, Pattern Recognition