Wakeling Emma L, Cruwys Michele, Suri Mohnish, Brady Angela F, Aylett Sarah E, Hall Christine
North West Thames Regional Genetics Service, Kennedy-Galton Centre, Level 8 V, North West London Hospitals NHS Trust, Watford Road, Harrow HAI 3UJ, Middlesex, UK.
Pediatr Radiol. 2004 Jul;34(7):541-6. doi: 10.1007/s00247-004-1207-7. Epub 2004 May 18.
Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder associated with defects in nucleotide excision repair. We report a 7-year-old boy with TTD due to mutation in the XPD gene. The patient has classic features of this condition, including brittle, sulphur-deficient hair, ichthyosis, growth retardation and developmental delay. In addition, he has radiological evidence of progressive central osteosclerosis. Although similar radiological findings have previously been reported in a small number of patients, this association is not widely recognised. We review the radiological findings in this and other similar cases and discuss the natural history of these bony changes.
毛发硫营养不良(TTD)是一种罕见的常染色体隐性多系统疾病,与核苷酸切除修复缺陷有关。我们报告一名7岁男孩,因XPD基因突变患有TTD。该患者具有此病的典型特征,包括脆弱、缺硫的毛发、鱼鳞病、生长发育迟缓。此外,他有进行性中央骨硬化的影像学证据。虽然此前在少数患者中报告过类似的影像学表现,但这种关联尚未得到广泛认可。我们回顾了该病例及其他类似病例的影像学表现,并讨论了这些骨质改变的自然病程。