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Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services
A teenage Afghan girl presented with seizure. Clinical features and laboratory investigations revealed elevated serum parathormone, high phosphate levels with low serum calcium. In third‐world countries, diagnosis of rare disorders, such as Albright hereditary osteodystrophy (AHO), can usually be de...
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842773/ https://www.ncbi.nlm.nih.gov/pubmed/36694647 http://dx.doi.org/10.1002/ccr3.6841 |