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xeroderma pigmentosum

[ pig-muhn-toh-suhm ]

noun

Pathology.
  1. a rare inherited disease characterized by sensitivity to ultraviolet light, exposure resulting in lesions and tumors of the skin and eyes.


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yvlog History and Origins

Origin of xeroderma pigmentosum1

1880–85; < New Latin: pigmented xeroderma; pigment, -ose 1
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Example Sentences

"The fact that CS proteins have additional functions is noteworthy. This discovery could help to explain the pathological differences between xeroderma pigmentosum and Cockayne syndrome," says Stingele.

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Figure 1 | Evidence of defective DNA repair in cells from people with xeroderma pigmentosum.

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For instance, some people are born with xeroderma pigmentosum, a rare, incurable genetic disorder in which the skin cannot repair the damage caused by ultraviolet light, leaving them vulnerable to cancer when they are children.

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The couple, who are Navajo, had two children with a severe form of xeroderma pigmentosum, or X.P., a genetic disorder, and then met other Navajo parents whose children had it as well.

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People with a rare inherited disorder called xeroderma pigmentosum have extreme sensitivity to the sun and must avoid exposure at all times.

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