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...

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Detalles Bibliográficos
Autores principales: Alhammadi, Ahmed H, Khalifa, Mohamed, Alnaimi, Lolwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Case Report
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

Internet

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

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