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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:...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
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| Materias: | |
| 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 |