Xeroderma pigmentosum is a genodermatosis characterized by photosensitivity and the development of cutaneous and internal malignancies at an early age. The basic defect underlying the clinical manifestations is a nucleotide excision repair defect, leading to defective repair of DNA damaged by ultraviolet radiation. These patients exhibit enhanced sensitivity to ionizing radiation. Patients with xeroderma pigmentosum who are younger than 20 years of age have a greater than 1000-fold increased risk of developing skin cancer. Early detection of these malignancies is necessary because they are fast growing, metastasize early and lead to death. Although, early detection and treatment of cutaneous malignancies will reduce the morbidity and mortal...
Xeroderma pigmentosum is a rare autosomal recessive genetic disorder characterized by defective DNA ...
Squamous cell carcinoma (SCC) of the skin usually occurs in older patients and commonly develops fro...
Xeroderma pigmentosum, or XP, is an autosomal recessive genetic disorder in which the ability to rep...
Xeroderma pigmentosum is a genodermatosis characterized by photosensitivity and the development of c...
Xeroderma pigmentosum (XP)is a rare inherited skin disorder characterized by a heightened sensitivit...
Malignant melanomas were found in 15.8% of xeroderma pigmentosum (XP) patients with skin cancer in J...
Pigmented xerodermoid, a rare genodermatosis, presents with clinical features and pathology similar...
Introduction: Xeroderma pigmentosum is a rare autosomal recessive genetic disease. This disease pred...
Xeroderma Pigmentosum is a rare, autosomal recessive genetic disorder, characterized by defective DN...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair. Affected individu...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
Background: Xeroderma pigmentosum (XP) is an autosomal recessive genetic disorder characterized by p...
Background. Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of UV radiation-induce...
Squamous cell carcinoma (SCC) of the skin usually occurs in older patients and commonly develops fr...
Abstract Xeroderma pigmentosum (XP) is defined by extreme sensitivity to sunlight, resulting in sunb...
Xeroderma pigmentosum is a rare autosomal recessive genetic disorder characterized by defective DNA ...
Squamous cell carcinoma (SCC) of the skin usually occurs in older patients and commonly develops fro...
Xeroderma pigmentosum, or XP, is an autosomal recessive genetic disorder in which the ability to rep...
Xeroderma pigmentosum is a genodermatosis characterized by photosensitivity and the development of c...
Xeroderma pigmentosum (XP)is a rare inherited skin disorder characterized by a heightened sensitivit...
Malignant melanomas were found in 15.8% of xeroderma pigmentosum (XP) patients with skin cancer in J...
Pigmented xerodermoid, a rare genodermatosis, presents with clinical features and pathology similar...
Introduction: Xeroderma pigmentosum is a rare autosomal recessive genetic disease. This disease pred...
Xeroderma Pigmentosum is a rare, autosomal recessive genetic disorder, characterized by defective DN...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair. Affected individu...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder of DNA repair characterized by su...
Background: Xeroderma pigmentosum (XP) is an autosomal recessive genetic disorder characterized by p...
Background. Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of UV radiation-induce...
Squamous cell carcinoma (SCC) of the skin usually occurs in older patients and commonly develops fr...
Abstract Xeroderma pigmentosum (XP) is defined by extreme sensitivity to sunlight, resulting in sunb...
Xeroderma pigmentosum is a rare autosomal recessive genetic disorder characterized by defective DNA ...
Squamous cell carcinoma (SCC) of the skin usually occurs in older patients and commonly develops fro...
Xeroderma pigmentosum, or XP, is an autosomal recessive genetic disorder in which the ability to rep...