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Reducing diagnostic delay in hypophosphatasia: a case series of 14 patients presenting to general rheumatology
OBJECTIVES: Hypophosphatasia (HPP) is a rare genetic metabolic bone disease that can cause chronic pain and fractures. Its hallmark is a persistently low serum ALP. HPP is now recognised by many osteoporosis specialists, but other specialists, such as rheumatologists and primary care physicians, may...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer London
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427523/ https://www.ncbi.nlm.nih.gov/pubmed/37118032 http://dx.doi.org/10.1007/s00198-023-06749-z |