Decoding IPEX Syndrome: From FOXP3 Mutation to Immunodysregulation
IPEX syndrome is a rare genetic disorder caused by mutations in the FOXP3 gene, crucial for regulatory T cell function. Symptoms include enteropathy, endocrinopathy, and dermatitis, appearing early in life. Management involves immunosuppressive therapy, symptom management, and potential hematopoietic stem cell transplantation. Research continues to explore treatment innovations and earlier diagnosis.… Read More Decoding IPEX Syndrome: From FOXP3 Mutation to Immunodysregulation


