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 ...

The condition is more common in Japan, North Africa, and the Middle East than in the United States or Europe. It’s typically diagnosed in infancy or early childhood. It can also be diagnosed ...

Xeroderma pigmentosum (XP) is the archetype of an expanding family of nucleotide-excision repair (NER) diseases that includes XP itself, the XP variant (XP-V), Cockayne syndrome (CS), cerebro ...

Affected populations: Xeroderma pigmentosum is a rare genetic disorder that makes people's skin extremely sensitive to the harmful effects of ultraviolet (UV) light. Both males and females can develop ...

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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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 ...

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.

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 ...