Demaerel P, Kendall B E, Kingsley D
Department of Neuroradiology, Hospital for Sick Children, London, UK.
Neuroradiology. 1992;34(2):117-21. doi: 10.1007/BF00588156.
The CT and MRI appearances of 5 patients with Cockayne's syndrome, 5 with ataxia telangiectasia and 1 with Fanconi's anaemia are reported. These conditions, together with Bloom's syndrome and xeroderma pigmentosum are regarded as disorders of DNA repair. Characteristic CT and MRI features of Cockayne's syndrome include generalised atrophy, calcification in basal ganglia and dentate nuclei and white matter low density. Neuroradiological findings in the other DNA repair disorders are nonspecific.
报告了5例科凯恩综合征、5例共济失调毛细血管扩张症和1例范科尼贫血患者的CT和MRI表现。这些病症,连同布卢姆综合征和着色性干皮病,被视为DNA修复障碍。科凯恩综合征的特征性CT和MRI表现包括全身性萎缩、基底神经节和齿状核钙化以及白质低密度。其他DNA修复障碍的神经放射学表现不具有特异性。