A Case Report of Rubinstein-Taybi Syndrome Presenting with Extensive Keloid Formation and Review of Literature.

Jee-Woo Kim, Jung Min Ko, Dong Yoon Lee, Jung-Won Shin
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Abstract

Rubinstein-Taybi syndrome (RSTS) is an extremely rare genetic disorder affecting multi-organ systems. A tendency to form keloid is one of the common dermatologic manifestations. We describe a 23-year-old female presented with extensive keloids which developed spontaneously. She had typical facial features, broad thumbs, and dental defects, which were suspicious features of genetic syndrome. Direct sequencing for cyclic-AMP-regulated enhancer binding protein revealed a novel mutation. So far, 23 cases of RSTS have been reported in Korean literature. To the best of our knowledge, this is the first report in Korea to describe confirmed case of RSTS with extensive keloids as a chief manifestation.

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Rubinstein-Taybi综合征伴广泛瘢痕疙瘩的病例报告及文献复习。
鲁宾斯坦-塔比综合征(RSTS)是一种影响多器官系统的极为罕见的遗传性疾病。瘢痕疙瘩的形成是常见的皮肤病表现之一。我们描述了一位23岁的女性,表现为广泛的瘢痕疙瘩,它是自发发展的。她有典型的面部特征、宽拇指和牙齿缺陷,这些都是遗传综合征的可疑特征。环腺苷酸调节增强子结合蛋白的直接测序揭示了一种新的突变。到目前为止,韩国文献中已经报道了23例RSTS病例。据我们所知,这是韩国首次报道以广泛瘢痕疙瘩为主要表现的RSTS确诊病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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