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Cockayne syndrome in two adult siblings.

作者信息

Miyauchi H, Horio T, Akaeda T, Asada Y, Chang H R, Ishizaki K, Ikenaga M

机构信息

Department of Dermatology, Kansai Medical University, Osaka, Japan.

出版信息

J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):329-35. doi: 10.1016/s0190-9622(94)70034-6.

Abstract

Although survival beyond the second decade is unusual in patients who have Cockayne syndrome, we describe two brothers with the syndrome who are 42 and 55 years of age. Their cultured skin fibroblasts showed extreme UV sensitivity but had almost normal UV-induced unscheduled DNA synthesis. The patients were classified as genetic complementation group B after study of the recovery of RNA synthesis after UV irradiation of fused cells. Clinical phototesting revealed a reduced threshold for UVB erythema.

摘要

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