Light protection for xeroderma pigmentosum

Ettinger, M. and Berneburg, M. (2017) Light protection for xeroderma pigmentosum. HAUTARZT, 68 (5). pp. 359-363. ISSN 0017-8470, 1432-1173

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Abstract

Xeroderma pigmentosum is a rare autosomal recessive disorder which is caused by germinal mutations responsible for the repair of ultraviolet (UV) radiation-induced DNA lesions. It is characterized by hypersensitivity to UV radiation, poikiloderma, ocular surface disease, and in some patients pronounced sunburn and neurological disease. Patients have a very high risk of developing ocular and skin cancer on exposed body sites. No cure is available for these patients except complete protection from all types of UV radiation.

Item Type: Article
Uncontrolled Keywords: DNA-REPAIR DEFICIENCY; COCKAYNE-SYNDROME; SKIN-CANCER; TRICHOTHIODYSTROPHY; HETEROGENEITY; PREVENTION; STRATEGIES; DISORDERS; MUTATIONS; DAMAGE; Genodermatosis; Light sensitivity; Poikiloderma; Tumors; Light protection
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Dermatologie und Venerologie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 14 Dec 2018 13:10
Last Modified: 18 Feb 2019 13:20
URI: https://pred.uni-regensburg.de/id/eprint/951

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