Since the material on XLH for PCPs and Aging with XLH in will be fairly long, I’m putting the footnotes here. Note that I’ve abbreviated the titles in some cases, rather than trying for formal citation format.
Footnote 1: “XLH Matters 2022”
Orphanet Journal of Rare Diseases
https://link.springer.com/article/10.1186/s13023-023-02883-3
Footnote 2: “XLH Matters: an evolving programme”
Orphatent Journal of Rare Diseases
https://link.springer.com/article/10.1186/s13023-024-03387-4
Footnote 3: “XLH Matters 2024”
Orphanet Journal of Rare Diseases
https://link.springer.com/article/10.1186/s13023-025-03930-x
Footnote 4: “XLH Management in Adults: Clinical Practice Guideline”
Journal of Clinical Endocrinology & Metabolism
https://pubmed.ncbi.nlm.nih.gov/40243526/
Footnote 5: “Clinical practice recommendations for the diagnosis and management of X-linked hypophosphatemia.”
Nature reviews Nephrology
https://pubmed.ncbi.nlm.nih.gov/39814982/
Footnote 6 : “XLH Management in Children”
Journal of Clinical Endocrinology & Metabolism
https://academic.oup.com/jcem/article/110/7/2055/8019634?login=false
Footnote 7: “Voice of the Patient report) from the Symposium on Hypophosphatemia, a 2018 Externally-Led Patient Focused Drug Development Meeting
https://xlhnetwork.org/wp-content/uploads/2023/05/VOP-XLH-Final.pdf
Footnote 8: National Cancer Institute (X-linked dominant transmission)
https://www.cancer.gov/publications/dictionaries/genetics-dictionary/def/x-linked-dominant-inheritance
Footnote 9: PHEX gene variant database: https://www.rarediseasegenes.com/x-linked-hypophosphatemia/genes-phex/
Footnote 10: Normal phosphorus from the UNC Medical Center: https://www.uncmedicalcenter.org/mclendon-clinical-laboratories/available-tests/phosphorus/
Footnote 11: Mayo Clinic Laboratories normals, https://www.mayocliniclabs.com/api/sitecore/TestCatalog/DownloadTestCatalog?testId=8408