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T. M. Rünger, J. J. DiGiovanna and K. H. Kraemer, “Hereditary Disorders of Genome Instability and DNA Repair,” In: K. Wolff, L. A. Goldsmith, S. I. Katz, et al., Eds., Fitzpatrick’s Dermatology in General Medicine, McGraw-Hill, New York, 2008, pp. 1311-1325.

has been cited by the following article:

• TITLE: Xeroderma Pigmentosum with Desquamative Gingivitis a Rare Case Report and Detailed Review of Literature

  AUTHORS: Shamimul Hasan, Mohammad Abbas Khan

  KEYWORDS: Oral Genodermatosis, Xeroderma Pigmentosum, Desquamative Gingivitis, Developmental Tongue Lesions

  JOURNAL NAME: Journal of Cosmetics, Dermatological Sciences and Applications, Vol.1 No.4, December 1, 2011

  ABSTRACT: In xeroderma pigmentosum, a rare genodermatosis, transmitted as an autosomal recessive disorder, excessive solar damage to the skin develops at an early age. The disease is characterized by cutaneous, ocular, neurological and oral changes. Oral features in the form of early development of Squamous cell carcinoma, usually at the lower lip and tip of the tongue may be seen. The disorder is associated more commonly in populations where marriage of close blood relatives is common. Treatment of the disorder includes avoidance of Ultra violet radiation, topical application of 5 fluorouracil to treat actinic keratoses, and regular evaluation by an optholmologist, dermatologist, and neurologist. Genetic counseling is an important aspect as an increased incidence of consanguineous marriages have been reported with this disorder. Here, we report an interesting case of xeroderma pigmentosum in an 18 year old male patient who presented with characterstic desquamation of gingiva, fissured tongue and geoghraphic tongue.