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Original Article

Pseudotumor cerebri as a presenting symptom of hypoparathyroidism in a thalassemia patient

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Pages 149-152 | Received 12 Sep 1984, Accepted 10 Apr 1985, Published online: 09 Jul 2009

References

  • Newns G H. Endocrinopathies in thalassemia major. Acta Paediatr Scand 1973; 62: 91
  • Flynn D M., Fairney A, Jackson D, Clayton B E. Hormonal changes in thalassemia major. Arch Dis Child 1976; 51: 828–36
  • McIntosh N. Endocrinopathy in thalassemia major. Arch Dis Child 1976; 51: 195–201
  • Madeddu G, Dore A, Marongiu A, Langer Constanzi M. Growth retardation skeletal maturation and thyroid function in children with homozygous B thalassemia. Clin Endocrinol 1978; 8: 359–65
  • Flatau E, Resnitzky P, Kauffman N, Harpaz S, Kohn D. Iron loading and endocrine functions in non transfused patients with B thalassemia intermedia or sickle cell thalassemia. Isr J Med Sci 1981; 17: 22–7
  • Oberklaid F, Seshadri R. Hyperparathyroidism and other endocrine dysfunction complicating thalassemia major. Med J Aust 1975; 1: 304–6
  • Gabrielle O. Hypoparathyroidism associated with thalassemia. South Med J 1971; 64: 115–16
  • Gertner J M., Broadus A E., Anast C S. Impaired parathyroid response to induced hypocalcemia in thalassemia major. J Pediatr 1979; 95: 210–13
  • Tsitoura S, Amarilio N, Lapatsanis P. Serum 25 hydroxyvitamin D levels in thalassemia. Arch Dis Child 1978; 53: 347–8
  • Aloia J F., Ostuni J A., Yeh J K., Zaino E C. Combined vitamin D parathyroid defect in thalassemia major. Arch Int Med 1982; 142: 831–2

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