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- W243065995 abstract "Congenital chloride losing enteropathy (familial chloride diarrhoea, congenital chloridorrhea)(1) is a recessively inherited disorder which results from a defect in chloride/bicarbonate exchange in the ileum. It is characterised by hydramnios in utero followed by lifelong osmotic diarrhoea. Inadequate fluid and electrolyte replacement can result in chronic hypokalaemic alkalosis, progressive renal insufficiency, drug resistant hyperuricaemia and gout.KeywordsAutosomal Recessive DiseaseUric Acid ExcretionUrine Uric AcidAcute Gouty ArthritisElectrolyte ReplacementThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves." @default.
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- W243065995 date "1991-01-01" @default.
- W243065995 modified "2023-09-27" @default.
- W243065995 title "Congenital Chloride Losing Enteropathy Associated with Tophaceous Gouty Arthritis" @default.
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- W243065995 doi "https://doi.org/10.1007/978-1-4899-2638-8_46" @default.
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