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Article

IPEX Syndrome: Genetics and Treatment Options.

Genes - 24 Feb 2021

Ben-Skowronek Iwona

Abstract excerpt

(1) Background: IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome characterizes a complex autoimmune reaction beginning in the perinatal period, caused by a dysfunction of the transcription factor forkhead box P3 (FOXP3). (2) Objectives: Studies have shown the clinical, immunological, and molecular heterogeneity of patients with IPEX syndrome. The symptoms, treatment, and survival...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33668198
DOI: 10.3390/genes12030323
PMCID: PMC7995986

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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