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Xeroderma pigmentosumA genetic disease that is characterized by such extraordinary sensitivity to sunlight that it results in the development of skin cancer at a very early age. Abbreviated XP. Children with XP can only play outdoors safely after nightfall. XP is due to defective repair of damage done to DNA by ultraviolet (UV) light. Whereas normal persons can repair [..]
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Xeroderma pigmentosumA genetic condition marked by an extreme sensitivity to ultraviolet radiation, including sunlight. People with xeroderma pigmentosum are not able to repair skin damage from the sun and other sources o [..]
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Xeroderma pigmentosuma syndrome acquired as an autosomal recessive trait and characterized by severe photosensitivity. It is elicited by a flaw in the capacity of the body to heal injury to DNA stemming from exposure to U [..]
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Xeroderma pigmentosumA genetic condition characterized by a sensitivity to all sources of ultraviolet radiation.
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Xeroderma pigmentosumA rare, pigmentary, and atrophic autosomal recessive Disease. It is manifested as an extreme photosensitivity to Ultraviolet Rays as the result of a deficiency in the enzyme that permits excisional re [..]
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Xeroderma pigmentosumA rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional re [..]
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Xeroderma pigmentosumA genetic condition marked by an extreme sensitivity to ultraviolet radiation, including sunlight. People with xeroderma pigmentosum are not able to repair skin damage from the sun and other sources of ultraviolet radiation, and have a very high risk of skin cancer.
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Xeroderma pigmentosumXeroderma Pigmentosum is a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn; inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light.
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Xeroderma pigmentosumA disease in human beings caused by a defect in the UV mutation repair system.
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