Neoplastic Disorder

Xeroderma Pigmentosum

AMW:DIS:040690

A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.

Pathology clinical

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Xeroderma Pigmentosum has parent DNA Repair-Deficiency Disorders

Xeroderma Pigmentosum has parent Photosensitivity Disorders

Xeroderma Pigmentosum has parent Pigmentation Disorders

Xeroderma Pigmentosum has parent Precancerous Conditions

Xeroderma Pigmentosum has parent Skin Abnormalities

Xeroderma Pigmentosum has parent Skin Diseases, Genetic

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