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Case Reports in Dentistry
Volume 2012, Article ID 840167, 3 pages
http://dx.doi.org/10.1155/2012/840167
Case Report

Familial Progressive Hyperpigmentation: A Case Report

1Department of Oral Pathology and Microbiology, Terna Dental College and Hospital, Sector No. 22, Nerul 400706, India
2Department of Periodontics, Terna Dental College and Hospital, Sector No. 22, Nerul 400706, India
3Department of Oral Pathology, Terna Dental College and Hospital, Sector No. 22, Nerul 400706, India

Received 19 January 2012; Accepted 28 February 2012

Academic Editors: P. G. Arduino, Y.-K. Chen, and A. Epivatianos

Copyright © 2012 Monica Yadav et al. 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. M. E. Chernosky, D. E. Anderson, J. P. Chang, M. W. Shaw, and M. M. Romsdahl, “Familial progressive hyperpigmentation,” Archives of Dermatology, vol. 103, no. 6, pp. 581–591, 1971. View at Publisher · View at Google Scholar · View at Scopus
  2. L. Zanardo, W. Stolz, G. Schmitz et al., “Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in South-East Germany,” Acta Dermato-Venereologica, vol. 84, no. 1, pp. 57–60, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. J. J. Norlund, The Pigmentary system, Genetic Epidermal Syndrome, Blackwell, Oxford University press, 2nd edition, 2006.
  4. A. Rebora and A. Parodi, “Universal inherited melanodyschromatosis: a case of melanosis universalis hereditaria?” Archives of Dermatology, vol. 125, no. 10, pp. 1442–1443, 1989. View at Google Scholar · View at Scopus
  5. L. Debao and L. Ting, “Familial progressive hyperpigmentation: a family study in China,” British Journal of Dermatology, vol. 125, no. 6, p. 607, 1991. View at Google Scholar · View at Scopus
  6. Z. Q. Wang, L. Si, Q. Tang et al., “Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation,” American Journal of Human Genetics, vol. 84, no. 5, pp. 672–677, 2009. View at Publisher · View at Google Scholar · View at Scopus
  7. R. Ruiz-Maldonado, L. Tamayo, and J. Fernandez-Diez, “Universal acquired melanosis. The carbon baby,” Archives of Dermatology, vol. 114, no. 5, pp. 775–778, 1978. View at Publisher · View at Google Scholar · View at Scopus
  8. G. Cardinali, D. Kovacs, M. Del Giglio et al., “A kindred with familial progressive hyperpigmentation-like disorder: implication of fibroblast-derived growth factors in pigmentation,” European Journal of Dermatology, vol. 19, no. 5, pp. 469–473, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. http://en.wikipedia.org/wiki/Hyperpigmentation.