Xeroderma pigmentosum (XP) is an extremely rare inherited condition affecting the skin and eyes. It is also referred to as DeSanctis-Cacchione syndrome. According to a quote, "People with xeroderma ...

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1. Which doctor should one consult to rule out Xeroderma pigmentosum? Normally parents would consult the GP or family physician for skin or eye problems, who may then refer them to a dermatologist ...

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Previous studies have demonstrated that p210 BCR/ABL1 interacts directly with the xeroderma pigmentosum group B (XPB) protein, and that XPB is phosphorylated on tyrosine in cells that express p210 BCR ...

Our genomic DNA is continuously damaged by endogenous factors such as reactive oxygen species, and also by environmental factors such as ultraviolet light, radiation, and chemicals. Failure to repair ...

Xeroderma pigmentosum (XP) is an autosomal recessive disease due to defective nucleotide excision repair (NER). The defects in XP patients fall into seven NER complementation groups: XP-A to XP-G and ...

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A rare inherited disorder, Xeroderma Pigmentosum (XP) is a photosensitive condition characterized by high susceptibility to skin cancers. XP follows the autosomal recessive pattern of inheritance.

Xeroderma pigmentosum (XP) is an inherited condition that causes extreme sensitivity to UV rays from the sun. It has been described as a 'one-in-a-million' condition. XP is brought on by a genetic ...

My Life: Into The Sun - Alice explains what it's like living with XP On Monday, a special episode of My Life will tell the story of Alice, 13, who lives with a rare genetic condition called xeroderma ...