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歌舞伎综合征:综述

Kabuki syndrome: a review.

作者信息

Adam M P, Hudgins L

机构信息

Division of Medical Genetics, Stanford University, Stanford, CA 94305-5208, USA.

出版信息

Clin Genet. 2005 Mar;67(3):209-19. doi: 10.1111/j.1399-0004.2004.00348.x.

Abstract

Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a multiple malformation/mental retardation syndrome that was described initially in Japan but is now known to occur in many other ethnic groups. 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, and mental retardation. A number of other manifestations involving other organ systems can aid in the diagnosis and management of KS. This review will focus on the diagnostic criteria, the common and rare features of KS by organ system, and the possible etiology of this interesting condition.

摘要

歌舞伎综合征(KS)(歌舞伎面容综合征、丹川-黑木综合征)是一种多发性畸形/智力发育迟缓综合征,最初在日本被描述,现在已知在许多其他种族群体中也有发生。其特征为独特的面部特征(下外侧眼睑外翻、外侧三分之一眉毛呈拱形且稀疏或分散、鼻尖凹陷、耳朵突出)、骨骼异常、皮纹异常、身材矮小和智力发育迟缓。涉及其他器官系统的许多其他表现有助于歌舞伎综合征的诊断和管理。本综述将重点关注诊断标准、按器官系统划分的歌舞伎综合征的常见和罕见特征,以及这种有趣病症的可能病因。

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