A: #XLH is caused by a pathogenic variant (mutation) on the X chromosome, which leads to the body's production of too much FGF23, which prevents the kidneys from sending phosphorus to the bloodstream. https://t.co/ec1hLtKJMd
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RT @Osteoporosis_NL: FGF23 and its role in X-linked hypophosphatemia-related morbidity. Beck- Nielsen SS et al. Orphanet J Rare Dis. 2019 F…
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RT @Osteoporosis_NL: FGF23 and its role in X-linked hypophosphatemia-related morbidity. Beck- Nielsen SS et al. Orphanet J Rare Dis. 2019 F…
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FGF23 and its role in X-linked hypophosphatemia-related morbidity. Beck- Nielsen SS et al. Orphanet J Rare Dis. 2019 Feb 26;14(1):58 https://t.co/h0WxmiQk1B ...excellent review https://t.co/aVWtmuS5VA