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He has a rare genetic disorder known as xeroderma pigmentosum.
Provides sharing of support, information and coping skills for families affected by xeroderma pigmentosum.
A rare genetic disease, xeroderma pigmentosum, has made Katie a prisoner of the dark.
He studied the development of cancer cells, in particular the skin cancer xeroderma pigmentosum.
More extraordinary than surviving twenty-eight years unscathed by xeroderma pigmentosum.
Xeroderma pigmentosum mostly affects the eye and skin.
Mutations in the protein commonly cause Xeroderma Pigmentosum which often lead to skin cancer.
Xeroderma pigmentosum is a group of rare skin disorders that makes the skin very sensitive to sunlight.
High-dose isotretinoin was found to prevent new skin cancers in individuals with xeroderma pigmentosum.
Christopher's experience of surfing is rather unusual: suffering from the genetic disorder xeroderma pigmentosum he cannot go out during the day, but only at night.
Sarasin A: Progress and prospects of xeroderma pigmentosum therapy.
Skin cancers commonly occur in people with the rare hereditary disorder, xeroderma pigmentosum, after exposure to sunlight.
Because xeroderma pigmentosum afflicts only one in a million people, sufferers can feel tremendous isolation at home, even torment.
Xeroderma pigmentosum, a skin disease.
He suffers from Xeroderma pigmentosum.
Kapture is the official celebrity spokesperson for the Xeroderma Pigmentosum Society.
Swift M, Chase C: Cancer in families with xeroderma pigmentosum.
The xeroderma pigmentosum paradigm.
Or other things that affect your skin, such as: Inherited genetic disorders, such as xeroderma pigmentosum.
A deficiency of excinuclease occurs in a rare autosomal recessive disease called xeroderma pigmentosum.
Snow, who was introduced to readers in "Fear Nothing," suffers from xeroderma pigmentosum, a rare intolerance to all but the dimmest light.
Xeroderma Pigmentosum Study Group.
Among them, xeroderma pigmentosum and Rothmund-Thomson syndrome (poikiloderma congenita) are thought to be the most prominent.
The special phone is just one of many steps Katie and her parents have taken to help her cope with xeroderma pigmentosum, or XP.