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Adv Rheumatol ; 64(1): 79, 2024 Oct 09.
Article in English | MEDLINE | ID: mdl-39385260

ABSTRACT

Systemic vasculitis is a group of rare diseases that share an essential characteristic: inflammation of blood vessel walls. This injury occurs during the disease course, but specific features vary for each entity. In this paper, we will address relevant aspects of the newest monogenic mutation vasculitis, such as deficiency of adenosine deaminase 2 (ADA2) and VEXAS syndrome (UBA1), and other relevant vasculitis, such as Cogan syndrome and Susac syndrome that may share some similarities with them.


Subject(s)
Adenosine Deaminase , Rare Diseases , Humans , Adenosine Deaminase/deficiency , Adenosine Deaminase/genetics , Cogan Syndrome/complications , Susac Syndrome/complications , Susac Syndrome/diagnosis , Systemic Vasculitis/diagnosis , Agammaglobulinemia/complications , Mutation , Vasculitis , Intercellular Signaling Peptides and Proteins
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