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P06 Think of hypophosphatasia if atypical fracture with persistent low ALP levels

INTRODUCTION: Hypophosphatasia (HPP), a rare, underdiagnosed metabolic genetic bone disease caused by diminished or absent expression of the tissue non-specific alkaline phosphatase (TNSALP) enzyme. The mutation of alkaline phosphatase (ALPL) gene leads to wide-ranging clinical manifestations, broad...

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Detalles Bibliográficos
Autores principales: Latheef, Afzal, Moss, Katie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532213/
http://dx.doi.org/10.1093/rap/rkad070.027