Familial Clustering of Juvenile Psoriatic Arthritis Associated with a Hemizygous FOXP3 Mutation

Curr Rheumatol Rep. 2021 Jul 3;23(8):64. doi: 10.1007/s11926-021-01026-6.

Abstract

Purpose of review: We describe the clinical and genetic findings in four patients from a single family who presented with refractory psoriatic arthritis and were hemizygous in the forkhead box protein 3 (FOXP3) gene (c.1222G>A).

Recent findings: We report four siblings with hemizygous mutation in the FOXP3 gene (c.1222G>A) who presented with type 1 diabetes mellitus and psoriatic arthritis poorly responsive to treatment. Our findings expand the phenotype spectrum of FOXP3 mutations. Immune dysregulation, polyendocrinopathy, and enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in FOXP3 gene, which lead to early onset of constellation of autoimmune manifestations. This report highlights the influence of immune dysregulation in juvenile arthritis.

Keywords: Diabetes mellitus; Hemizygous FOXP3; IPEX; Immune dysregulation; Juvenile arthritis; Psoriatic arthritis.

Publication types

  • Review

MeSH terms

  • Arthritis, Juvenile* / genetics
  • Cluster Analysis
  • Forkhead Transcription Factors / genetics
  • Genetic Diseases, X-Linked* / genetics
  • Humans
  • Mutation
  • T-Lymphocytes, Regulatory

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors