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Hypophosphatemic osteomalacia demonstrated by Tc-99m MDP bone scan: a case report.

Authors
Kim, S; Park, CH; Chung, YS
Citation
Clinical nuclear medicine, 25(5):337-340, 2000
Journal Title
Clinical nuclear medicine
ISSN
0363-97621536-0229
Abstract
Hypophosphatemic osteomalacia, a familial or rarely acquired disorder, is characterized biochemically by hypophosphatemia, decreased renal tubular reabsorption of phosphate, decreased intestinal absorption of calcium, and normal serum calcium. This report concerns a rare case of hypophosphatemic osteomalacia of unknown cause that was shown on Tc-99m MDP bone scanning.
MeSH terms
AdultBone and Bones/radionuclide imagingHumansHypophosphatemia, Familial/*radionuclide imagingMaleOsteomalacia/*radionuclide imagingTechnetium Tc 99m Medronate/diagnostic use
PMID
10795690
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
Journal Papers > School of Medicine / Graduate School of Medicine > Nuclear Medicine & Molecular Imaging
AJOU Authors
박, 찬희정, 윤석
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