Abstract
Vitamin D resistant hypophosphataemic osteomalacia (VDRHPO) occurs as an inherited disorder or more unusually in association with certain connective tissue tumours1. The primary defect is considered to be a failure of phosphate transport with decreased tubular phosphate reabsorption and hypophosphataemia resulting in osteomalacia and myopathy2.
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References
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© 1977 Springer Science+Business Media New York
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Peacock, M., Aaron, J.E., Heyburn, P.J., Nordin, B.E.C. (1977). The Action of 1αhydroxy Vitamin D3 and Phosphate Supplements in Hypophosphataemic Osteomalacia. In: Massry, S.G., Ritz, E. (eds) Phosphate Metabolism. Advances in Experimental Medicine and Biology, vol 81. Springer, New York, NY. https://doi.org/10.1007/978-1-4613-4217-5_44
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DOI: https://doi.org/10.1007/978-1-4613-4217-5_44
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