Xeroderma pigmentosum, which is commonly known as XP, is an inherited condition characterized by an extreme sensitivity to ultraviolet (UV) rays from sunlight.
Xeroderma pigmentosum, or XP, is an autosomal recessive genetic disorder of DNA repair in which the ability to repair damage caused by ultraviolet (UV) light is ...
Xeroderma pigmentosum (XP) was first described in 1874 by Hebra and Kaposi. In 1882, Kaposi coined the term xeroderma pigmentosum for the condition ...
Xeroderma pigmentosum What is xeroderma pigmentosum? Xeroderma pigmentosum (XP) is a very rare skin disorder where a person is highly sensitive to sunlight ...
What is xeroderma pigmentosum? Xeroderma pigmentosum (XP) is a hereditary condition characterized by extreme sun sensitivity, leading to a very high risk of skin cancer.
It is possible that the main title of the report Xeroderma Pigmentosum is not the name you expected. Please check the synonyms listing to find the ...
Xeroderma pigmentosum is an autosomal recessive disorder. This means you must have two copies of an abnormal gene in order for the disease or trait to develop.
Programs The Xeroderma Pigmentosum Society runs a number of programs including education, fundraising, and outreach to benefit those affected by XP around the world.
Xeroderma Pigmentosum: symptoms, cause, treatments, complications, prevention, risks. MamasHealth.com: simple, easy to understand information about health. Skin Health :
Information about xeroderma pigmentosum, an inherited disease that causes sun sensitivity, including its symptoms, diagnosis, and treatment.