IPEX syndrome (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) is a very rare inherited condition where regulatory T cells (Treg) CD4 CD25 are lacking due to a mutation in the FoxP3 gene, leading to the development of autoimmunity.
El síndrome IPEX es una afección heredada muy rara donde faltan células T reguladoras (Treg) CD4 CD25 debido a una mutación en el gen FoxP3, lo que lleva al desarrollo de autoinmunidad.
| Front | Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. A very rare inherited condition in which CD4 CD25 regulatory Tregcells are lacking as a result of a mutation in the gene for the transcription factor FoxP3, leading to the development of autoimmunity |
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| Back | IPEX immune dysregulation, polyendocrinopathy, enteropathy, X-linked |
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