Literature DB >> 17437133

Hyperostosis with hyperphosphatemia and tumoral calcinosis: a case report.

Hasan Otukesh1, Rozita Hoseini, Hamid Chalian, Majid Chalian, Amir Ebrahim Safarzadeh, Marjan Shakiba, Ali Poorian.   

Abstract

The combination of hyperostosis and hyperphosphatemia is very rare. In this case report, we present a boy with a combination of diffuse hyperostosis and hyperphosphatemia. We evaluated most possible known causes of hyperphosphatemia and hyperostosis. He had normal renal function and serum parathormone level. Concerning some few similar cases, most of them from Middle Eastern countries, we present this combination (diffuse hyperostosis and hyperphosphatemia) as a new syndrome to be discussed in pediatric textbooks.

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Year:  2007        PMID: 17437133     DOI: 10.1007/s00467-007-0476-4

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  11 in total

Review 1.  Disorders of phosphate metabolism.

Authors:  L A DiMeglio; K E White; M J Econs
Journal:  Endocrinol Metab Clin North Am       Date:  2000-09       Impact factor: 4.741

2.  Hyperphosphatemia associated with cortical hyperostosis and tumoral calcinosis.

Authors:  M P Wilson; C B Lindsley; B A Warady; J A Johnson
Journal:  J Pediatr       Date:  1989-06       Impact factor: 4.406

3.  Renal adaptation to dietary phosphate deprivation: role of proximal tubule brush-border membrane fluidity.

Authors:  B S Levine; K A Knibloe; K Golchini; S Hashimoto; I Kurtz
Journal:  Am J Physiol       Date:  1991-05

Review 4.  PHEX gene and hypophosphatemia.

Authors:  M K Drezner
Journal:  Kidney Int       Date:  2000-01       Impact factor: 10.612

Review 5.  FGF23: its role in renal bone disease.

Authors:  Masafumi Fukagawa; Junichiro James Kazama
Journal:  Pediatr Nephrol       Date:  2006-08-24       Impact factor: 3.714

6.  Cortical hyperostosis with hyperphosphatemia: a new syndrome?

Authors:  R E Melhem; S S Najjar; A K Khachadurian
Journal:  J Pediatr       Date:  1970-12       Impact factor: 4.406

7.  Tumoral calcinosis: a case report and review of the literature.

Authors:  S F Viegas; E B Evans; J Calhoun; S E Goodwiller
Journal:  J Hand Surg Am       Date:  1985-09       Impact factor: 2.230

8.  Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

Authors:  Orit Topaz; Daniel L Shurman; Reuven Bergman; Margarita Indelman; Paulina Ratajczak; Mordechai Mizrachi; Ziad Khamaysi; Doron Behar; Dan Petronius; Vered Friedman; Israel Zelikovic; Sharon Raimer; Arieh Metzker; Gabriele Richard; Eli Sprecher
Journal:  Nat Genet       Date:  2004-05-09       Impact factor: 38.330

9.  Phosphorus excretion in tumoral calcinosis: response to parathyroid hormone and acetazolamide.

Authors:  E G Lufkin; D M Wilson; L H Smith; N J Bill; H F DeLuca; T P Dousa; F G Knox
Journal:  J Clin Endocrinol Metab       Date:  1980-04       Impact factor: 5.958

10.  Cloning and expression of cDNA for a Na/Pi cotransport system of kidney cortex.

Authors:  A Werner; M L Moore; N Mantei; J Biber; G Semenza; H Murer
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

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  1 in total

Review 1.  Familial tumoral calcinosis and the role of O-glycosylation in the maintenance of phosphate homeostasis.

Authors:  Ilana Chefetz; Eli Sprecher
Journal:  Biochim Biophys Acta       Date:  2008-10-25
  1 in total

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