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史密斯-马吉尼斯综合征的面容:一项主观与客观研究。

The face of Smith-Magenis syndrome: a subjective and objective study.

作者信息

Allanson J E, Greenberg F, Smith A C

机构信息

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.

出版信息

J Med Genet. 1999 May;36(5):394-7.

Abstract

We report a study of 55 subjects with Smith-Magenis syndrome, aged 9 months to 35 years. Each person has been evaluated with an assessment of "gestalt" and detailed facial measurement, using previously published methodology, with compilation of Z score pattern profiles. The facial phenotype of SMS is quite distinctive, even in the young child. The overall face shape is broad and square. The brows are heavy, with excessive lateral extension of the eyebrows. The eyes slant upwards and appear close set and deep set. The nose has a depressed root and, in the young child, a scooped bridge. With time, the bridge becomes more ski jump shaped. The height of the nose is markedly reduced while the nasal base is broad and the tip of the nose is full. The shape of the mouth and upper lip are most distinctive. The mouth is wide with full upper and lower lips. The central portion of the upper lip is fleshy and everted with bulky philtral pillars, producing a tented appearance that, in profile, is striking. With age, mandibular growth is greater than average and exceeds that of the maxilla. This leads to increased jaw width and protrusion and marked midface hypoplasia. Craniofacial pattern analysis supports these subjective impressions. After mid-childhood, mandibular dimensions consistently exceed their maxillary counterparts. Craniofacial widths are greater than corresponding depths and heights. Nasal height is reduced while nasal width is increased. There is mild brachycephaly. The most marked age related changes are increased width of the nose and lower face (mandibular width) with reduction in nasal height and midfacial depth.

摘要

我们报告了一项对55名年龄在9个月至35岁之间的史密斯-马吉尼斯综合征患者的研究。每个人都使用先前发表的方法,通过“整体”评估和详细的面部测量进行了评估,并编制了Z评分模式档案。即使在幼儿中,史密斯-马吉尼斯综合征的面部表型也非常独特。整体面部形状宽阔且呈方形。眉毛浓密,眉梢过度向外延伸。眼睛向上倾斜,看起来眼距近且深陷。鼻子根部凹陷,在幼儿中鼻梁呈勺状。随着时间的推移,鼻梁变得更像滑雪跳台的形状。鼻子高度明显降低,而鼻基底宽阔,鼻尖饱满。嘴巴和上唇的形状最为独特。嘴巴宽阔,上、下唇饱满。上唇中央部分肉质且外翻,鼻唇沟支柱粗大,形成一种帐篷状外观,从侧面看非常明显。随着年龄增长,下颌生长大于平均水平,超过上颌。这导致下颌宽度增加和前突,以及明显的面中部发育不全。颅面模式分析支持了这些主观印象。童年中期之后,下颌尺寸始终超过上颌。颅面宽度大于相应的深度和高度。鼻高降低而鼻宽增加。有轻度短头畸形。最明显的与年龄相关的变化是鼻子和下脸(下颌宽度)变宽,同时鼻高和面中部深度减小。

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本文引用的文献

1
Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2).
Am J Med Genet. 1998 Mar 28;81(2):186-91.
2
Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).史密斯-马吉尼斯综合征(17p11.2缺失)的行为表型
Am J Med Genet. 1998 Mar 28;81(2):179-85. doi: 10.1002/(sici)1096-8628(19980328)81:2<179::aid-ajmg10>3.0.co;2-e.
3
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2).史密斯-马吉尼斯综合征(17p11.2缺失)的多学科临床研究
Am J Med Genet. 1996 Mar 29;62(3):247-54. doi: 10.1002/(SICI)1096-8628(19960329)62:3<247::AID-AJMG9>3.0.CO;2-Q.
4
Anthropometric craniofacial pattern profiles in Down syndrome.
Am J Med Genet. 1993 Oct 1;47(5):748-52. doi: 10.1002/ajmg.1320470530.
6
Applications of pattern profile analysis to malformations of the head and face.
Radiology. 1984 Mar;150(3):683-90. doi: 10.1148/radiology.150.3.6695067.

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