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...

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Detalles Bibliográficos
Autores principales: Rauf, Muhammad A., Kotecha, Jalpa, Moss, Katie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2023
Materias:
Short Communication
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

Internet

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

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