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 ...

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 (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 ...

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.