Cho Eunhe, Yang Tae Hwan, Shin Eun-Sim, Byeon Jung Hye, Kim Gun-Ha, Eun Baik-Lin
Childs Nerv Syst. 2013 Nov;29(11):2101-4. doi: 10.1007/s00381-013-2235-0.
Saethre–Chotzen syndrome is a very rare autosomal dominant congenital disorder characterized by craniosynostosis and acrocephalosyndactyly. It is caused by a mutation in TWIST1, located on chromosome 7p21. A shortage of functional TWIST1 protein affects the development and maturation of cells in the skull, face, and limbs. The patient described in this report displayed craniofacial features classic for Saethre–Chotzen syndrome, including craniosynostosis, low-set ears, small pinna with prominent crura, a high-arched palate, and a simian crease on the left hand. He did not have the limb anomalies commonly seen in patients with Saethre–Chotzen syndrome, and the results of conventional chromosome analysis were normal. However, results of a microarray-based comparative genomic hybridization (array CGH) study confirmed the karyotype of46,XY.7p21.1p15.3(15,957,375-20,331,837)x1, a region that includes TWIST1. Subsequent fluorescent in situ hybridization analysis confirmed this result. No other chromosome was involved in the rearrangement. This case illustrates the important contribution of array CGH to the identification of TWIST microdeletions, even in a patient not showing the phenotype typical of Saethre–Chotzen syndrome.
塞特勒-乔岑综合征是一种非常罕见的常染色体显性先天性疾病,其特征为颅缝早闭和尖头并指畸形。它由位于7号染色体p21区域的TWIST1基因突变引起。功能性TWIST1蛋白的缺乏会影响颅骨、面部和四肢细胞的发育与成熟。本报告中描述的患者表现出塞特勒-乔岑综合征典型的颅面特征,包括颅缝早闭、低位耳、耳廓小且耳轮突出、高拱腭以及左手猿线。他没有塞特勒-乔岑综合征患者常见的肢体异常,常规染色体分析结果正常。然而,基于微阵列的比较基因组杂交(阵列CGH)研究结果证实其核型为46,XY.7p21.1p15.3(15,957,375 - 20,331,837)x1,该区域包含TWIST1。随后的荧光原位杂交分析证实了这一结果。没有其他染色体参与重排。该病例说明了阵列CGH在识别TWIST微缺失方面的重要作用,即使在未表现出塞特勒-乔岑综合征典型表型的患者中也是如此。