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Xeroderma pigmentosum.
Lehmann AR, McGibbon D, Stefanini M. Lehmann AR, et al. Orphanet J Rare Dis. 2011 Nov 1;6:70. doi: 10.1186/1750-1172-6-70. Orphanet J Rare Dis. 2011. PMID: 22044607 Free PMC article. Review.
Estimated incidences vary from 1 in 20, 000 in Japan to 1 in 250, 000 in the USA, and approximately 2.3 per million live births in Western Europe.The first features are either extreme sensitivity to sunlight, triggering severe sunburn, or, in patients who do not show this sun-sen …
Estimated incidences vary from 1 in 20, 000 in Japan to 1 in 250, 000 in the USA, and approximately 2.3 per million live births in Western E …
Molecular genetics of Xeroderma pigmentosum variant.
Gratchev A, Strein P, Utikal J, Sergij G. Gratchev A, et al. Exp Dermatol. 2003 Oct;12(5):529-36. doi: 10.1034/j.1600-0625.2003.00124.x. Exp Dermatol. 2003. PMID: 14705792 Review.
Xeroderma pigmentosum (XP) is an autosomal recessive disease characterized by sun sensitivity, early onset of freckling and subsequent neoplastic changes on sun-exposed skin. Skin abnormalities result from an inability to repair UV-damaged DNA b …
Xeroderma pigmentosum (XP) is an autosomal recessive disease characterized by sun sensitivity, early onset of freckling and subsequent neopl …
Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan.
Yamamura K, Ichihashi M, Hiramoto T, Ogoshi M, Nishioka K, Fujiwara Y. Yamamura K, et al. Br J Dermatol. 1989 Oct;121(4):471-80. doi: 10.1111/j.1365-2133.1989.tb15514.x. Br J Dermatol. 1989. PMID: 2696553 Review.
The patient had mild clinical symptoms consisting of numerous pigmented freckles and a small number of seborrheic keratosis-like papules. She had no skin cancers in the sun-exposed areas of the skin and so far no neurological abnormalities
The patient had mild clinical symptoms consisting of numerous pigmented freckles and a small number of seborrheic keratosis-like papu …