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

ABSTRACT 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 ex...

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Detalhes bibliográficos

Principais autores:	Craig F Munns, Han‐Wook Yoo, Muhammad Yazid Jalaludin, Rashida Vasanwala, Manju Chandran, Yumie Rhee, Wai Man BUT, Alice Pik‐Shan Kong, Pen‐Hua Su, Nawaporn Numbenjapon, Noriyuki Namba, Yasuo Imanishi, Roderick J Clifton‐Bligh, Xiaoping Luo, Weibo Xia
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Oxford University Press 2023-06-01
coleção:	JBMR Plus
Assuntos:	X‐LINKED HYPOPHOSPHATEMIC RICKETS CARE TRANSITION PRACTICE GUIDELINES ASIA ASIA‐PACIFIC
Acesso em linha:	https://doi.org/10.1002/jbm4.10744
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