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

机译:歌舞uki彩妆综合症–肌电图研究病例报告

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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uki化妆综合症(KMS),也称为新川黑木综合症,发生于1981年,是一种罕见的先天性疾病,病因不明。尽管最初在日本描述过,但已知在许多其他种族中也有发生。我们报告根据特征性临床特征诊断出患有歌舞uki综合症的亚洲裔24岁女孩。它的特征是独特的面部特征(下眼睑外翻,侧面三分之一的弓形眉毛散布或稀疏,鼻尖凹陷和突出的耳朵),骨骼异常,皮纹异常,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,本报告强调其作用。

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