Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries

INTRODUCTION: X-linked hypophosphatemia (XLH) is a rare inherited cause of hypophosphatemic rickets and osteomalacia. It is caused by mutations in the phosphate-regulating endopeptidase homolog, X-linked (PHEX). This results in increased plasma fibroblast growth factor-23 (FGF23), which leads to los...

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Detalles Bibliográficos
Autores principales: Al Juraibah, Fahad, Al Amiri, Elham, Al Dubayee, Mohammed, Al Jubeh, Jamal, Al Kandari, Hessa, Al Sagheir, Afaf, Al Shaikh, Adnan, Beshyah, Salem A., Deeb, Asma, Habeb, Abdelhadi, Mustafa, Manal, Zidan, Hanaa, Mughal, M. Zulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2021
Materias:
Consensus Statement
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929956/
https://www.ncbi.nlm.nih.gov/pubmed/33660084
http://dx.doi.org/10.1007/s11657-021-00879-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929956/
https://www.ncbi.nlm.nih.gov/pubmed/33660084
http://dx.doi.org/10.1007/s11657-021-00879-9

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