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Kabuki Make-up Syndrome – A Case Report with Electromyographic study

机译:歌舞伎化妆综合症:肌电图研究的病例报告

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摘要

Kabuki make-up syndrome (KMS), also called Niikawa-Kuroki syndrome reported in 1981, is a rare congenital disorder of unknown aetiology. It is know to occur in many other ethnic groups, though initially described in Japan. We report a 24-year-old girl of Asian origin diagnosed with Kabuki syndrome based on characteristic clinical features. It is characterized by distinctive facial features (eversion of the lower lateral eyelid, arched eyebrows with the lateral one-third dispersed or sparse, depressed nasal tip, and prominent ears), skeletal anomalies, Dermatoglyphic abnormalities, short stature. As per our knowledge there is no literature which gives information about the importance of electromyographic study in the diagnosis and treatment of the KMS. Hence, this report emphasizes on the role of the same.
机译:歌舞伎化妆综合征 (KMS),也称为 1981 年报道的新川黑木综合征,是一种病因不明的罕见先天性疾病。众所周知,它发生在许多其他民族中,尽管最初是在日本描述的。我们报告了一名 24 岁的亚裔女孩,根据特征性临床特征被诊断患有歌舞伎综合征。其特征是明显的面部特征(下侧眼睑外翻、眉毛呈拱形,外侧三分之一分散或稀疏、鼻尖凹陷和耳朵突出)、骨骼异常、皮形畸形、身材矮小。据我们所知,没有文献提供有关肌电图研究在 KMS 诊断和治疗中的重要性的信息。因此,本报告强调了其作用。

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