Suppr超能文献

克拉克-巴拉伊泽综合征:一例新病例报告及文献综述

Clark-Baraitser syndrome: report of a new case and review of the literature.

作者信息

Mendicino Angela, Sabbadini Guglielmo, Pergola Mariano S

机构信息

U.O. di Genetica, Dipartimento Materno Infantile, ASL RME, Rome, Italy Istituto PRODA, Rome, Italy.

出版信息

Clin Dysmorphol. 2005 Jul;14(3):133-135.

Abstract

We describe the case of a boy with moderate mental retardation associated with tall stature, obesity, macrocephaly and typical facial features, characterized by a large 'square' forehead, prominent supraorbital ridges, broad nasal tip, prominent lower lip and minor dental anomalies. We think that our proband is affected by Clark-Baraitser syndrome, a rare X-linked mental retardation disorder, to date described only in five male subjects. We present a more complete definition of the clinical phenotype of the syndrome with particular attention to the behavioural aspect that, in combination with the body size and the dysmorphic picture, we think is distinctive for the Clark-Baraitser syndrome. We also summarize the mild features described in female relatives of the patients, as it could disclose a possible carrier condition and be of help with genetic counselling in the families with male patients, until a molecular test is available.

摘要

我们描述了一名患有中度智力障碍的男孩的病例,其伴有身材高大、肥胖、巨头畸形和典型的面部特征,特点为宽大的“方形”前额、突出的眶上嵴、宽阔的鼻尖、突出的下唇以及轻微的牙齿异常。我们认为我们的先证者患有克拉克-巴拉伊泽综合征,这是一种罕见的X连锁智力障碍疾病,迄今为止仅在五名男性受试者中被描述过。我们给出了该综合征临床表型的更完整定义,特别关注行为方面,我们认为结合体型和畸形特征,这对于克拉克-巴拉伊泽综合征具有独特性。我们还总结了在患者女性亲属中描述的轻微特征,因为这可能揭示一种潜在的携带者状态,并有助于对男性患者家庭进行遗传咨询,直到有可用的分子检测方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验