Medical Definition of Xeroderma pigmentosum

  • Medical Author:
    William C. Shiel Jr., MD, FACP, FACR

    Dr. Shiel received a Bachelor of Science degree with honors from the University of Notre Dame. There he was involved in research in radiation biology and received the Huisking Scholarship. After graduating from St. Louis University School of Medicine, he completed his Internal Medicine residency and Rheumatology fellowship at the University of California, Irvine. He is board-certified in Internal Medicine and Rheumatology.

Reviewed on 10/30/2018

Xeroderma pigmentosum: A genetic disease that is characterized by such extraordinary sensitivity to sunlight that it results in the development of skin cancer at a very early age. Abbreviated XP. Children with XP can only play outdoors safely after nightfall. XP is due to defective repair of damage done to DNA by ultraviolet (UV) light. Whereas normal persons can repair UV-induced damage by inserting new bases into the DNA, XP patients cannot. A person with XP develops severe sunburn and eye irritation within minutes of exposure to sunlight. Other features of XP include very dry skin (xeroderma), blisters on the skin, heavy freckling, and dark spots on the skin. XP is inherited in an autosomal recessive manner. Defects in multiple genes have been identified that lead to XP. Avoiding UV light and using the highest level of sunscreen possible when exposure cannot be avoided helps prevent complications.

CONTINUE SCROLLING OR CLICK HERE FOR RELATED ARTICLE

Health Solutions From Our Sponsors

Reviewed on 10/30/2018