Atypical Presentations of IPEX: Expect the Unexpected
Immune dysregulation, polyendocrinopathy, and enteropathy, X-linked (IPEX) syndrome is a rare disorder that has become a model of monogenic autoimmunity. IPEX is caused by mutations in FOXP3 gene, a master regulator of regulatory T cells (Treg). Cases reported in the last 20 years demonstrate that I...
Main Authors: | Filippo Consonni, Sara Ciullini Mannurita, Eleonora Gambineri |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-02-01
|
Series: | Frontiers in Pediatrics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2021.643094/full |
Similar Items
-
IL-2 Signaling Axis Defects: How Many Faces?
by: Filippo Consonni, et al.
Published: (2021-07-01) -
Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Immune Dysregulatory Disorders
by: Shahrzad Bakhtiar, et al.
Published: (2019-11-01) -
IPEX syndrome: Case report
by: Radlović Nedeljko, et al.
Published: (2008-01-01) -
IPEX Syndrome: Improved Knowledge of Immune Pathogenesis Empowers Diagnosis
by: Federica Barzaghi, et al.
Published: (2021-02-01) -
Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?
by: Micaela Gentile, et al.
Published: (2022-04-01)