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Case Reports

Clinical status of Sagliker syndrome: a case report and literature review

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Pages 800-803 | Received 09 Oct 2013, Accepted 26 Jan 2014, Published online: 27 Feb 2014

References

  • Sagliker Y, Balal M, Sagliker Ozkaynak P, et al. Sagliker syndrome: uglifying human face appearance in late and severe secondary hyperparathyroidism in chronic renal failure. Semin Nephrol. 2004;24(5):449–455
  • Sagliker Y, Acharya V, Ling Z, et al. International study on Sagliker syndrome and uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic kidney disease patients. J Ren Nutr. 2008;18(1):114–117
  • Dantas M, Costa RS, Jorgetti V, et al. Facial leontiasis ossea: a rare presentation of hyperparathyroidism secondary to chronic renal insufficiency. Nephron. 1991;58(4):475–478
  • Lee VS, Webb MS Jr, Martinez S, et al. Uremic leontiasis ossea: “bighead” disease in humans? Radiologic, clinical, and pathologic features. Radiology. 1996;199(1):233–240
  • Fisher D, Hiller N, Drukker A. Nephroquiz for the beginner: a swollen face in a girl on hemodialysis. Diagnosis: renal osteodystrophy. Nephrol Dial Transplant. 1999;14(7):1797–1798
  • Yildiz I, Sagliker Y, Demirhan O, et al. International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4. J Ren Nutr. 2012;22(1):157–161
  • Wang M, You L, Li H, et al. Association of circulating fibroblast growth factor-23 with renal phosphate excretion among hemodialysis patients with residual renal function. Clin J Am Soc Nephrol. 2013;8(1):116–125

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