Jiménez-Puya R, Moreno-Giménez J C, Camacho-Martínez F, Ferrando-Barbera J, Grimalt R
Servicio de Dermatología, Hospital Universitario Reina Sofía, Córdoba, España.
Actas Dermosifiliogr. 2007 Apr;98(3):183-7.
Trichothiodystrophy comprises a heterogeneous group of autosomal recessive entities. This fact gives rise to different interrelated neuroectodermal disorders. From a structural point of view these features are the result of the low tissue sulfur content. We report a case of trichothiodystrophy initially classified as Tay syndrome that based on clinical features, complementary exams as well as on the disease evolution was labelled as PIBIDS syndrome.
毛发硫营养不良症是一组常染色体隐性疾病的异质性疾病。这一事实引发了不同的相互关联的神经外胚层疾病。从结构角度来看,这些特征是组织硫含量低的结果。我们报告了一例最初被归类为Tay综合征的毛发硫营养不良症病例,该病例基于临床特征、辅助检查以及疾病进展被标记为PIBIDS综合征。