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Kabuki make‐up syndrome and hearing impairment

机译:歌舞伎化妆综合症和听力障碍

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In 1981, Nnkawa 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.
机译:1981 年,Nnkawa 等人和 Kuroki 等人独立描述了一种新综合征患者,包括智力低下、出生后生长缺陷和不寻常的面部特征,例如长睑裂伴下眼睑外翻三分之一、眉毛呈拱形和侧向稀疏以及大而突出的耳朵等畸形。这种情况被称为歌舞伎化妆综合症,因为受影响个体的面部特征类似于日本戏剧中演员的化妆:歌舞伎。在对日本个体的初步报告之后,在其他几名不同种族的患者中观察到了这种情况,包括来自该国的一些患者(Kaiser-Kupfer等人,1986;Pagon等人,1986)。我们描述了另一名患有歌舞伎化妆综合症的 13 岁男性患者,可能暗示其母亲的常染色体显性遗传 有趣的是,我们的患者还表现出迄今为止未报告的严重听骨畸形,导致严重的听力障碍。

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