Definition of "xeroderma" noun: a mild form of ichthyosis characterized by abnormal dryness and roughness of the skin

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	WikiPedia definition of "xeroderma" Xeroderma pigmentosum, or XP, is an autosomal recessive genetic disorder of DNA repair in which the ability to repair damage caused by ultraviolet (UV) light is deficient. (More) Xeroderma (literally "dry skin") is a condition involving the integumentary system, which in most cases can safely be treated with emollients and/or moisturizers. (More) Décrit en 1870 [1] par Moritz Kaposi, le xeroderma pigmentosum est une photodermatose d' origine génétique rare. Elle se caractérise par une sensibilité excessive de la peau ... (More) XPB (Xeroderma Pigmentosum B) is an ATP dependent human DNA helicase that is a part of the TFIIH transcription factor complex. (More) Xeroderma pigmentosum (oder synonym Melanosis lenticularis progressiva, auch Mondscheinkrankheit oder Lichtschrumpfhaut, kurz XP) ist eine Hautkrankheit, die auf einem genetischen ... (More) Xeroderma pigmentosum, complementation group C, also known as XPC, is a human gene involved in the recognition of bulky DNA adducts in Nucleotide Excision Repair. References (More) Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G (Cockayne syndrome)), also known as ERCC5, is ... (More) The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases.". Genes Dev. 15 (1): 15–23. PMID 11156600.   Benhamou S, Sarasin A (2003). (More) Xanthic urolithiasis; Xanthine oxydase deficiency; Xanthinuria; Xanthomatosis cerebrotendinous; Xerocytosis, hereditary; Xeroderma pigmentosum, type 1; Xeroderma pigmentosum, type 2; Xeroderma ... (More) It is milder than Type I and II. Xeroderma-pigmentosum-Cockayne syndrome (XP-CS) occurs when an individual also suffers from Xeroderma pigmentosum, another DNA repair disease. (More)

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