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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:...
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| Udgivet i: | Ann Med Surg (Lond) |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7840437/ https://ncbi.nlm.nih.gov/pubmed/33537138 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amsu.2021.01.067 |
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