hyperphosphatasemia

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Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.

Saki F, Karamizadeh Z, Nasirabadi S, Mumm S, McAlister WH, Whyte MP.SourceDepartment of Pediatric Endocrinology, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran; Student Research Committee, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.J Bone Miner Res.2013 Jun;28(6):1501-8. doi: 10.1002/jbmr.1868.
Juvenile Paget's disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline phosphatase (ALP) activity emanating from generalized acceleration of skeletal turnover. Affected infants and children typically suffer bone pain and fractures and deformiti
PMID 23322328

Li J, Molnar MZ, Zaritsky JJ, Sim JJ, Streja E, Kovesdy CP, Salusky I, Kalantar-Zadeh K.SourceHarold Simmons Center for Chronic Disease Research and Epidemiology, University of California Irvine Medical Center, Irvine, CA, USA.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.Nephrol Dial Transplant.2013 Jun;28(6):1516-25. doi: 10.1093/ndt/gfs598. Epub 2013 Jan 24.
BACKGROUND: The implications of chemical hyperparathyroidism on bone and mineral metabolism measures in maintenance hemodialysis (MHD) are not well known. We hypothesized that a higher serum intact parathyroid hormone (iPTH) level is associated with the higher likelihood of hyperphosphatemia, hyperp
PMID 23348879

DORI Neta,LEVI Lily,STAM Tamar,SUKHOTNIK Igor,SHAOUL Ron
Pediatrics international : official journal of the Japan Pediatric Society 52(6), 866-871, 2010-12-01
NAID 10028184772