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Case Reports in Neurological Medicine
Volume 2011, Article ID 407567, 4 pages
Case Report

Intracranial Hemorrhage Revealing Pseudohypoparathyroidism as a Cause of Fahr Syndrome

Department of Medicine, Silchar Medical College, Silchar, Assam, 788014, India

Received 14 July 2011; Accepted 9 August 2011

Academic Editors: S. T. Gontkovsky and Y. Narita

Copyright © 2011 Abhijit Swami and Giridhari Kar. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. L. C. Wilson and C. M. Hall, “Albright's hereditary osteodystrophy and pseudohypoparathyroidism,” Seminars in Musculoskeletal Radiology, vol. 6, no. 4, pp. 273–283, 2002. View at Google Scholar · View at Scopus
  2. Y. Nakamura, T. Matsumoto, A. Tamakoshi et al., “Prevalence of idiopathic hypoparathyroidism and pseudohypoparathyroidism in Japan,” Journal of Epidemiology, vol. 10, no. 1, pp. 29–33, 2000. View at Google Scholar · View at Scopus
  3. N. Kahloul, W. Chaari, L. Boughamoura, L. Charfeddine, S. Khammeri, and F. Amri, “Pseudohypoparathyroidism revealed by Fahr syndrome,” Archives de Pediatrie, vol. 16, no. 5, pp. 444–448, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  4. M. G. Harrington, P. Macpherson, W. B. McIntosh, B. F. Allam, and I. Bone, “The significance of the incidental finding of basal ganglia calcification on computed tomography,” Journal of Neurology Neurosurgery and Psychiatry, vol. 44, no. 12, pp. 1168–1170, 1981. View at Google Scholar
  5. B. V. Manyam, “What is and what is not 'Fahr's disease',” Parkinsonism and Related Disorders, vol. 11, no. 2, pp. 73–80, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  6. Y. Baba, D. F. Broderick, R. J. Uitti, M. L. Hutton, and Z. K. Wszolek, “Heredofamilial brain calcinosis syndrome,” Mayo Clinic Proceedings, vol. 80, no. 5, pp. 641–651, 2005. View at Google Scholar · View at Scopus
  7. L. Morgante, G. Vita, and M. Meduri, “Fahr's syndrome: local inflammatory factors in the pathogenesis of calcification,” Journal of Neurology, vol. 233, no. 1, pp. 19–22, 1986. View at Google Scholar
  8. Y. Otheman, H. Khalloufi, I. Benhima, and A. Ouanass, “Neuropsychiatric symptoms revealing pseudohypoparathyroidism with Fahr's syndrome,” Encephale, vol. 37, no. 1, pp. 54–58, 2011. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  9. S. J. Siejka, W. V. Knezevic, and P. T. Pullan, “Dystonia and intracerebral calcification: pseudohypoparathyroidism presenting in an eleven-year-old girl,” Australian and New Zealand Journal of Medicine, vol. 18, no. 4, pp. 607–609, 1988. View at Google Scholar · View at Scopus
  10. J. T. Potts Jr., “Diseases of the parathyroid gland and other hyper- and hypocalcemic disorders,” in Harrison's Principles of Internal Medicine, vol. 2, p. 2394, McGraw–Hill, New York, NY, USA, 17th edition, 2008. View at Google Scholar
  11. M.-L. Kotter, A. Linglart, and J.-C. Carel, “Albright hereditary osteodystrophy,” Orphanet Encyclopedia, January 2004,
  12. A. S. Balavoine, M. Ladsous, F. L. Velayoudom et al., “Hypothyroidism in patients with pseudohypoparathyroidism type Ia: clinical evidence of resistance to TSH and TRH,” European Journal of Endocrinology, vol. 159, no. 4, pp. 431–437, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  13. W. Stögmann, “Pseudohypoparathyroidism with hypothyroidism,” Padiatrie und Padologie, vol. 16, no. 4, pp. 403–409, 1981. View at Google Scholar
  14. S. D. Cederbaum and B. M. Lippe, “Probable autosomal recessive inheritance in a family with Albright's hereditary osteodystrophy and an evaluation of the genetics of the disorder,” American Journal of Human Genetics, vol. 25, no. 6, pp. 638–645, 1973. View at Google Scholar · View at Scopus
  15. B. V. Manyam, “Bilateral strio-pallido-dentate calcinosis. Proposed classifications of genetic and secondary causes,” Movement Disorders, vol. 5, pp. 94–97, 1990. View at Google Scholar
  16. M. Şenoglu, D. Tunclel, F. Ö. Orhan, Z. Yuksel, and M. Gockce, “Fahr’s syndrom: a report of two cases,” Fırat Tıp Dergisi, vol. 12, no. 1, pp. 70–72, 2007. View at Google Scholar
  17. S. B. Zachariah, B. Zachariah, N. Antonios, and L. D. Prockop, “Pseudohypoparathyroidism and cerebrovascular disease with dural calcification,” Journal of the Florida Medical Association, vol. 78, no. 1, pp. 26–28, 1991. View at Google Scholar · View at Scopus