Article
A Case of Autoimmune Fanconi Syndrome Secondary to Ipex Syndrome
2024-08-26
Abstract excerpt
<title>Abstract</title> <p><bold>Background:</bold> IPEX syndrome ir a rare monogenic autoimmune disorder resulting from mutations in the FOXP3 gene. This condition is typified by severe early-onset autoimmunity, typically presenting as a triad encompassing enteropathy, polyendocrinopathy, and eczema. Renal involvement is less common. <bold>Case Description:</bold> One-year-old male exhibiting enteropathy, endocr...
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Identifiers and source
- Literature Corpus work
- 5364bdfb-a7e5-5aa1-9ebe-d78aef0033c0
- DOI
- 10.21203/rs.3.rs-4749977/v1
