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XLH Diagnosis checklist

X-linked hypophosphatemia (XLH) is a rare hereditary but lifelong and progressive disease.1 Early diagnosis and treatment are important for better treatment outcomes.1,2

Find out with the below easy-to-use checklist if you or your loved ones need to see a doctor for XLH screening.

References: 1. Munns CF, et al. Asia-Pacific Consensus Recommendations on X-Linked Hypophosphatemia: Diagnosis, Multidisciplinary Management, and Transition From Pediatric to Adult Care. JBMR Plus. 2023 May 1;7(6):e10744. doi: 10.1002/jbm4.10744. 2. Hamdy NAT, et al. X-linked hypophosphatemia: The medical expert’s challenges and the patient’s concerns on their journey with the disease. Arch Pediatr. 2021 Oct;28(7):612-618. doi: 10.1016/j.arcped.2021.09.005.

AP-NP-24-00002 JAN2024

XLH 連結 - 醫護人員網站

本協和麒麟網站的適用對象為有負責照護性聯遺傳低血磷症 (XLH) 患者的專業醫護人員 (HCP)。


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