SAT-376 Secondary Hyperparathyroidism, an Untoward Complication of High Dose Phosphate Supplementation in Hereditary Hypophosphatemic Rickets

Background: Hereditary hypophosphatemic rickets is a debilitating disease with multiple skeletal abnormalities. Children exhibit rickets and growth failure, while adults exhibit bone pain, enthesopathy, HTN, and arthritis. Gene mutations involving renal phosphate reabsorption(PHEX, FGF23, SLC34A3) l...

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Vydáno v:J Endocr Soc
Hlavní autoři: Pinjala, Anusha, Gastelum, Alheli Arce, Adel Maraqa, Sima Abdel Rahman, Samec, Joshua, Zena, Mohsen
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2020
Témata:
Bone and Mineral Metabolism
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208970/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.744
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