Suspect XLH?
Connect their symptoms and accurately diagnose with the right tests.
XLH is primarily an inherited condition, which means it runs in families.3
New symptoms of XLH may appear as patients get older and can worsen or change over time.4
Individuals with XLH can continue to experience symptoms throughout their lives.4
Connect their symptoms and accurately diagnose with the right tests.
Manage XLH early to prevent progressive bone damage.
From case studies to brochures, find resources for you and your patients to understand more about this rare condition.
Set up time with a representative to talk more about XLH, or sign up for news and information about XLH.
References:
1. Giannini S, Bianchi ML, Rendina D, Massoletti P, Lazzerini D, Brandi ML. Burden of disease and clinical targets in adult patients with X-linked hypophosphatemia. A comprehensive review. Osteoporos Int. 2021;32(10):1937-1949. doi:10.1007/s00198-021-05997-1 2. Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL. A clinician's guide to X-linked hypophosphatemia. J Bone Miner Res. 2011;26(7):1381-1388. doi:10.1002/jbmr.340 3. Ruppe MD. X-linked hypophosphatemia. In: Adam MP, Everman DB, Mirzaa GM, et al., eds. GeneReviews®. Seattle (WA): University of Washington, Seattle; February 9, 2012. Updated April 13, 2017. https://www.ncbi.nlm.nih.gov/books/NBK83985/ 4. Skrinar A, Dvorak-Ewell M, Evins A, et al. The lifelong impact of X-linked hypophosphatemia: results from a burden of disease survey. J Endocr Soc. 2019;3(7):1321-1334. doi:10.1210/js.2018-00365