Autoimmune Polyendocrine Syndromes in the Pediatric Age.
autoantibodies
autoimmune
children
immunodeficiency
pediatrics
polyendocrinopathy
polyglandular
Journal
Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936
Informations de publication
Date de publication:
19 Mar 2023
19 Mar 2023
Historique:
received:
07
02
2023
revised:
13
03
2023
accepted:
17
03
2023
medline:
30
3
2023
entrez:
29
3
2023
pubmed:
30
3
2023
Statut:
epublish
Résumé
Autoimmune polyendocrine syndromes (APSs) encompass a heterogeneous group of rare diseases characterized by autoimmune activity against two or more endocrine or non-endocrine organs. Three types of APSs are reported, including both monogenic and multifactorial, heterogeneous disorders. The aim of this manuscript is to present the main clinical and epidemiological characteristics of APS-1, APS-2, and IPEX syndrome in the pediatric age, describing the mechanisms of autoimmunity and the currently available treatments for these rare conditions.
Identifiants
pubmed: 36980146
pii: children10030588
doi: 10.3390/children10030588
pmc: PMC10047132
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
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