Xeroderma pigmentosum (XP) is a rare genetic disease that affects young children. These young patients, called children of ...

At risk individuals include: Transplant recipients (solid organ and stem cell) Genetic syndrome patients (Gorlin's, Rombo, Bazex, xeroderma pigmentosum, Muir-Torre) Lymphoma patients (non-Hodgkin ...

These disorders include ataxia-telangiectasia (AT), a degenerative motor condition caused by failure to repair oxidative damage in the cerebellum, and xeroderma pigmentosum (XP), a condition ...