Xeroderma Pigmentosum in Children: Report of 4 Cases

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MIRI ALIABAD GHASEM; ASGARZADEH LEILA

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Health Scope Year:2020 | Volume:9 | Issue:4 Page(s): 0-0

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Title

Xeroderma Pigmentosum in Children: Report of 4 Cases

Author(s)

MIRI ALIABAD GHASEM | ASGARZADEH LEILA | Issue Writer Certificate

Keywords

Xeroderma Pigmentosum

Photosensitivity

Melanoma

DNA Repair

Abstract

Xeroderma Pigmentosum (XP) is a rare genetic disorder inherited in an autosomal recessive pattern. Patients with XP are extremely sensitive to ultraviolet (UV) radiation that leads to defective DNA Repair. People with XP often suffer from problems in the eyes, face, neck, and other areas of the body, frequently exposed to sunlight. It is characterized by Photosensitivity, dry skin, pigmentary changes of the skin, premature skin aging, and a considerable increase in incidence rates of malignant skin tumors. There is no cure for XP. In this article, we have described four patients from two families, three of whom had malignant skin tumors.

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APA: Copy

MIRI ALIABAD, GHASEM, & ASGARZADEH, LEILA. (2020). Xeroderma Pigmentosum in Children: Report of 4 Cases. HEALTH SCOPE, 9(4), 0-0. SID. https://sid.ir/paper/982666/en

Vancouver: Copy

MIRI ALIABAD GHASEM, ASGARZADEH LEILA. Xeroderma Pigmentosum in Children: Report of 4 Cases. HEALTH SCOPE[Internet]. 2020;9(4):0-0. Available from: https://sid.ir/paper/982666/en

IEEE: Copy

GHASEM MIRI ALIABAD, and LEILA ASGARZADEH, “Xeroderma Pigmentosum in Children: Report of 4 Cases,” HEALTH SCOPE, vol. 9, no. 4, pp. 0–0, 2020, [Online]. Available: https://sid.ir/paper/982666/en

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