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歌舞伎综合征与听力障碍。

Kabuki make-up syndrome and hearing impairment.

作者信息

Say B, McCutcheon L, Todd C, Hough J V

机构信息

H. Allen Chapman Research Institute of Medical Genetics, Children's Medical Center, Tulsa, OK 74135.

出版信息

Clin Dysmorphol. 1993 Jan;2(1):68-70.

PMID:8298741
Abstract

In 1981, Niikawa et al. and Kuroki et al. independently described patients with a new syndrome consisting of mental retardation, postnatal growth deficiency and unusual facial features such as long palpebral fissures with eversion of the lateral one-third of the lower eyelids, arched and laterally sparse eyebrows and large prominent ears among other malformations. The condition has been called Kabuki make-up syndrome because the facial features in affected individuals resemble the make-up of the actors in a Japanese play: Kabuki. After the initial reports on Japanese individuals, the condition has been observed in several other patients of different ethnic origins including a few patients from this country (Kaiser-Kupfer et al., 1986; Pagon et al., 1986). We describe an additional 13-year-old male patient with Kabuki make-up syndrome with possible implication of autosomal dominant inheritance from his mother. Interestingly, our patient also displayed hitherto unreported severe ossicular malformations resulting in significant hearing impairment.

摘要

1981年,新川等人和黑木等人分别描述了一种患有新综合征的患者,该综合征包括智力迟钝、出生后生长发育迟缓以及不寻常的面部特征,如睑裂长、下眼睑外侧三分之一外翻、眉毛呈弓形且外侧稀疏、耳朵大而突出等其他畸形。这种病症被称为歌舞伎化妆综合征,因为受影响个体的面部特征类似于日本戏剧《歌舞伎》中演员的妆容。在最初关于日本个体的报道之后,在其他几个不同种族的患者中也观察到了这种病症,包括本国的一些患者(凯泽 - 库普弗等人,1986年;帕贡等人,1986年)。我们描述了一名额外的13岁男性歌舞伎化妆综合征患者,其可能从母亲那里遗传了常染色体显性遗传特征。有趣的是,我们的患者还表现出了迄今未报道的严重听小骨畸形,导致了明显的听力障碍。

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