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lüll Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome Wildin RS; Smyk-Pearson S; Filipovich AHJ Med Genet 2002[Aug]; 39 (8): 537-45Immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX, OMIM 304790) is a rare, recessive disorder resulting in aggressive autoimmunity and early death. Mutations in FOXP3 have been identified in 13 of 14 patients tested. Research in the mouse model, scurfy, suggests that autoimmunity may stem from a lack of working regulatory T cells. We review published reports regarding the genetics, clinical features, immunology, pathology, and treatment of IPEX. We also report three new patients who were treated with long term immunosuppression, followed by bone marrow transplantation in two. IPEX can be differentiated from other genetic immune disorders by its genetics, clinical presentation, characteristic pattern of pathology, and, except for high IgE, absence of substantial laboratory evidence of immunodeficiency. While chronic treatment with immunosuppressive drugs may provide temporary benefit for some patients, it does not cause complete remission. Remission has been observed with bone marrow transplantation despite incomplete engraftment, but the long term outcome is uncertain.|Adolescent[MESH]|Animals[MESH]|Autoimmune Diseases/*diagnosis/*genetics/radiotherapy/therapy[MESH]|Child[MESH]|Child, Preschool[MESH]|Diabetes Mellitus, Type 1/diagnosis/genetics/radiotherapy/therapy[MESH]|Diagnosis, Differential[MESH]|Disease Models, Animal[MESH]|Humans[MESH]|Lymphoproliferative Disorders/diagnosis/genetics/radiotherapy/therapy[MESH]|Male[MESH]|Polyendocrinopathies, Autoimmune/diagnosis/genetics/radiotherapy/therapy[MESH]|Protein-Losing Enteropathies/*genetics/*immunology/radiotherapy/therapy[MESH]|Syndrome[MESH] |