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 ...

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 ...

Xeroderma pigmentosum, or XP, is a rare genetic disorder that prevents the skin from repairing sun damage. There are about 300 Americans currently living with XP, and the chances of being born in this ...

>> I NEED TO WEAR A JACKET. JESSICA: STACY PEREZ NEVER DRESSES FOR THE WEATHER. >> MY HAT. AND GLOVES. JESSICA: HER ONLY CONCERN ON THIS HOT AND HUMID DAY, PROTECTING HER BODY FROM ULTRAVIOLET LIGHT.

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 ...

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 ...

Desde los 10 años, Deíde Freire de Andrade vive con tantos problemas en la piel que hasta perdió su nariz. Ahora lleva una prótesis. Andrade es uno de los 17 habitantes de Recanto das Araras, un ...

Xeroderma Pigmentosum (XP) es una la enfermedad rara que afecta a unas 100 personas en toda España y que obliga a los ...

A woman with a rare genetic condition has shared how she wears a mask that looks like a 'space helmet' to protect her skin from damaging UV rays - and hasn't left the house without it for 20 years. At ...

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 ...