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Xeroderma pigmentosum and keratoconus.

作者信息

Blanksma L J, Donders P C, van Voorst Vader P C

出版信息

Doc Ophthalmol. 1986 Dec 30;64(1):97-103. doi: 10.1007/BF00166690.

DOI:10.1007/BF00166690
PMID:3556116
Abstract

Two XP patients are presented. A corneal perforation in the left eye of the first patient necessitated an at-random transplantation à chaud. The graft was remarkably well tolerated, which is possibly explained by UV-light-induced suppression of the cellular immune response in the patient. The right eye of this patient and both eyes of the second patient had a keratoconus. Keratoconus in XP may be the result of disturbances in the cell differentiation and the function of epithelial cells and keratocytes, due to UV-light-induced deficient DNA repair synthesis.

摘要

相似文献

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Xeroderma pigmentosum and keratoconus.
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引用本文的文献

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Indian J Ophthalmol. 2021 Apr;69(4):860-864. doi: 10.4103/ijo.IJO_2188_20.
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Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literature.着色性干皮病的眼部表现和组织病理学:两例临床病理病例及文献复习。
Surv Ophthalmol. 2011 Jul-Aug;56(4):348-61. doi: 10.1016/j.survophthal.2011.03.001.
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Sunlight, DNA damage and skin cancer: a new perspective.

本文引用的文献

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Graefes Arch Clin Exp Ophthalmol. 1991;229(4):395-400. doi: 10.1007/BF00170700.
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Ocular manifestations of xeroderma pigmentosum in a black family.
Arch Ophthalmol. 1974 Aug;92(2):113-7. doi: 10.1001/archopht.1974.01010010119007.
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Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.着色性干皮病。一种遗传性疾病,对阳光敏感,有多种皮肤肿瘤,且DNA修复异常。
Ann Intern Med. 1974 Feb;80(2):221-48. doi: 10.7326/0003-4819-80-2-221.