Monogenic familial autoinflammatory Behçet-like syndrome/ haploinsufficiency A20 syndrome is a new form of autoinflammatory pathology. Literature review and description of cases

Monogenic familial autoinflammatory Behçet-like syndrome/ haploinsufficiency A20 syndrome is a new form of autoinflammatory pathology. Literature review and description of cases

Monogenic familial autoinflammatory Behçet-like syndrome/haploinsufficiency A20 syndrome is a hereditary autoinflammatory disease from the group of ubiquitinopathies which are caused by a mutation of the TNFAIP3 gene encoding the A20 protein with an autosomal dominant inheritance mechanism and clini...

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Bibliographic Details
Main Authors: Е. S. Fedorov, S. О. Salugina, Е. Yu. Zakharova, А. N. Shapovalenko, S. G. Radenska-Lopovok, V. G. Matkava, А. N. Arefieva
Format: Article
Language:Russian
Published: IMA PRESS LLC 2024-04-01
Series:Научно-практическая ревматология
Subjects:
genetics
autoinflammatory diseases
tnfaip3 gene
a20 haploinsufficiency
relopathies
behçet’s disease
Online Access:https://rsp.mediar-press.net/rsp/article/view/3552
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