X-linked hypophosphatemic osteomalacia with PHEX mutation presenting late in Pakistan

ABSTRACT.INTRODUCTION.AND.IMPORTANCE: Autosomal dominant hypophosphatemic rickets is the most common form of rare rickets, commonly manifests in children but sometimes the condition remains undiagnosed due to lack of knowledge &/or awareness of treating physicians or surgeons. CASE PRESENTATION:...

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Detalles Bibliográficos
Autores principales: Zehra, Nawazish, Jafri, Lena, Kirmani, Salman, Khan, Aysha Habib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840437/
https://www.ncbi.nlm.nih.gov/pubmed/33537138
http://dx.doi.org/10.1016/j.amsu.2021.01.067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840437/
https://www.ncbi.nlm.nih.gov/pubmed/33537138
http://dx.doi.org/10.1016/j.amsu.2021.01.067

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