PHEX Gene Mutation in a Patient with X-Linked Hypophosphatemic Rickets in a Developing Country

INTRODUCTION: X-linked hypophosphatemic rickets is part of a larger group of hereditary diseases characterized by renal phosphate loss, which causes growth disorders, rickets, and osteomalacia. These conditions are characterized by disorders in phosphate equilibrium, which is essential for bone form...

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Detalles Bibliográficos
Autores principales: Forero-Delgadillo, Jessica María, Cleves, Daniela, Ochoa, Vanessa, Londoño-Correa, Hernando, Restrepo, Jaime Manuel, Nastasi-Catanese, José Antonio, Pachajoa, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025672/
https://www.ncbi.nlm.nih.gov/pubmed/32104046
http://dx.doi.org/10.2147/TACG.S232448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025672/
https://www.ncbi.nlm.nih.gov/pubmed/32104046
http://dx.doi.org/10.2147/TACG.S232448

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