Correcting hypophosphataemia in a paediatric patient with Sanjad–Sakati syndrome through a single oral dose of potassium phosphate intravenous solution

Sanjad–Sakati syndrome is an autosomal recessive disorder that is quite common in Kuwait. Among a wide range of complications in Sanjad–Sakati syndrome patients is the vulnerability to infections and subsequent hypophosphataemia. Hypophosphataemia is a metabolic alteration that contributes to numero...

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Detalles Bibliográficos
Autores principales: Sabti, Mnaff A, Shamsaldeen, Yousif A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812393/
https://www.ncbi.nlm.nih.gov/pubmed/33505699
http://dx.doi.org/10.1177/2050313X20988412

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812393/
https://www.ncbi.nlm.nih.gov/pubmed/33505699
http://dx.doi.org/10.1177/2050313X20988412

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