Asia‐Pacific Consensus Recommendations on X‐Linked Hypophosphatemia: Diagnosis, Multidisciplinary Management, and Transition From Pediatric to Adult Care

X‐linked hypophosphatemia (XLH) is a rare, inherited, multisystem disorder characterized by hypophosphatemia that occurs secondary to renal phosphate wasting. Mutations in PHEX gene (located at Xp22.1) in XLH alter bone mineral metabolism, resulting in diverse skeletal, dental, and other extraskelet...

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Detalles Bibliográficos
Autores principales: Munns, Craig F, Yoo, Han‐Wook, Jalaludin, Muhammad Yazid, Vasanwala, Rashida, Chandran, Manju, Rhee, Yumie, BUT, Wai Man, Kong, Alice Pik‐Shan, Su, Pen‐Hua, Numbenjapon, Nawaporn, Namba, Noriyuki, Imanishi, Yasuo, Clifton‐Bligh, Roderick J, Luo, Xiaoping, Xia, Weibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241092/
https://www.ncbi.nlm.nih.gov/pubmed/37283655
http://dx.doi.org/10.1002/jbm4.10744

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241092/
https://www.ncbi.nlm.nih.gov/pubmed/37283655
http://dx.doi.org/10.1002/jbm4.10744

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