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

被引:2
|
作者
Kim, Jee-Woo [1 ]
Ko, Jung Min [2 ]
Lee, Dong Yoon [3 ]
Shin, Jung-Won [1 ]
机构
[1] Seoul Natl Univ, Dept Dermatol, Bundang Hosp, Seongnam, South Korea
[2] Seoul Natl Univ, Dept Pediat, Childrens Hosp, Seoul, South Korea
[3] Dankook Univ Hosp, Dept Dermatol, Cheonan, South Korea
关键词
Base sequence; Cicatrix; Gene; Keloid; Rubinstein-Taybi syndrome; MUTATIONS; PATIENT;
D O I
10.5021/ad.20.320
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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.
引用
收藏
页码:S19 / S24
页数:6
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