Tolmie J L, de Berker D, Dawber R, Galloway C, Gregory D W, Lehmann A R, McClure J, Pollitt R J, Stephenson J B
Duncan Guthrie Institute of Medical Genetics, Yorkhill Hospital, Glasgow, Scotland, UK.
Clin Dysmorphol. 1994 Jan;3(1):1-14.
Sparse, brittle, sulphur-deficient hair is an excellent marker for several autosomal recessive neurocutaneous syndromes. The term 'trichothiodystrophy' is commonly used in publications on such syndromes and the best characterized trichothiodystrophy syndrome is associated with skin photosensitivity and intellectual impairment. Patients with these three cardinal signs usually have an underlying DNA repair defect. Here we describe clinical and laboratory findings in two patients with trichothiodystrophy and defective DNA repair alongside findings in three other cases who have different trichothiodystrophy syndromes without defective DNA repair. These patients' features are discussed in the light of a practical classification scheme which is based upon a check-list of clinical abnormalities associated with trichothiodystrophy syndromes (Van Neste, 1991).
稀疏、脆弱、缺硫的头发是几种常染色体隐性遗传神经皮肤综合征的一个重要标志。“毛发硫营养不良”一词在关于此类综合征的出版物中常用,最具特征的毛发硫营养不良综合征与皮肤光敏性和智力障碍有关。有这三个主要症状的患者通常存在潜在的DNA修复缺陷。在此,我们描述了两名毛发硫营养不良且DNA修复缺陷患者的临床和实验室检查结果,以及另外三名患有不同毛发硫营养不良综合征但无DNA修复缺陷患者的检查结果。根据基于与毛发硫营养不良综合征相关临床异常清单的实用分类方案(Van Neste,1991)对这些患者的特征进行了讨论。