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An infant with poor weight gain and hypochloremic metabolic alkalosis: a case report
Bartter syndrome is an autosomal recessive disease manifested by a defect in chloride transport in the thick loop of Henle, with different genetic origins and molecular pathophysiology. Children with Bartter syndrome generally present in early infancy with persistent polyuria and associated dehydrat...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122223/ https://www.ncbi.nlm.nih.gov/pubmed/25114583 http://dx.doi.org/10.2147/IJGM.S66550 |