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 ...

Pol Dominguez, 11, is enjoying his summer holidays in Spain. But unlike most children his age, he does not spend his days at the beach or pool, instead staying indoors to avoid ultraviolet radiation ...

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 ...

Optical illusion: Only a person with high intelligence can spot the smiley face Optical illusion: Only a person who has perfect vision can spot 3 differences in the guy cutting the tree 5 foods that ...

Most people can't wait for the long, warm days of summer to return. But for one young woman, being out in the sunshine is a nightmare she must actively avoid. Andrea Monroy, 23, was born with ...

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 a rare genetic condition affecting DNA repair. People with xeroderma pigmentosum are extremely ...

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 ...