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- W4313593322 abstract "Infantile refractory diarrhea presents after first few days of life leading to intestinal insufficiency. It is a diagnostic challenge due to varied etiologies like food senstive enteropathy, anatomical defects and dysmotility disorders, transport and enzymatic defects, pancreatic malabsorption - cystic fibrosis (CF), primary epithelial causes like microvillus inclusion disease (MVID), tufting enteropathy and heparan sulfate deficiency, immunodeficiencies, metabolic diseases and autoimmune enteropathy. It is refractory to treatment making the patient dependent on total parenteral nutrition. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), is one of the rarest causes of intractable diarrhea. It occurs due to mutations in the FOXP3 gene, leading to dysfunction of T-regulatory cells and is characterised by diarrhoea, diabetes, and dermatitis. We aim to evaluate various causes of infantile refractory chronic diarrhea, and to present one such case of IPEX syndrome from this part of the world due to mutation not been reported in literature so far." @default.
- W4313593322 created "2023-01-06" @default.
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- W4313593322 date "2023-01-01" @default.
- W4313593322 modified "2023-09-27" @default.
- W4313593322 title "Diagnostic dilemma in infantile refractory diarrhea: a rare case of IPEX syndrome" @default.
- W4313593322 cites W1998157143 @default.
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- W4313593322 doi "https://doi.org/10.1016/j.mjafi.2022.11.006" @default.
- W4313593322 hasPublicationYear "2023" @default.
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