Butler M G, Pratesi R, Watson M S, Breg W R, Singh D N
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2578.
Clin Genet. 1993 Sep;44(3):129-38. doi: 10.1111/j.1399-0004.1993.tb03863.x.
Anthropometric and craniofacial profile patterns indicating the percent difference from the overall mean were developed on 34 physical parameters with 31 white, mentally retarded males (23 adults and 8 children) with the fra(X) syndrome matched for age with 31 white, mentally retarded males without a known cause of their retardation. The fra(X) syndrome males consistently showed larger dimensions for all anthropometric variables, with significant differences for height, sitting height, arm span, hand length, middle finger length, hand breadth, foot length, foot breadth, and testicular volume. A craniofacial pattern did emerge between the two groups of mentally retarded males, but with overlap of several variables. Significant differences were noted for head circumference, head breadth, lower face height, bizygomatic diameter, inner canthal distance, ear length and ear width, with the fra(X) syndrome males having larger head dimensions (head circumference, head breadth, head length, face height and lower face height), but smaller measurements for minimal frontal diameter, bizygomatic diameter, bigonial diameter, and inner canthal distance. Several significant correlations were found with the variables for both mentally retarded males with and without the fra(X) syndrome. In a combined anthropometric and craniofacial profile of 19 variables comparing 26 white fra(X) syndrome males (13 with high expression (> 30%) and 13 with low expression (< 30%), but matched for age), a relatively flat profile was observed with no significant differences for any of the variables. Generally, fra(X) syndrome males with increased fragile X chromosome expression have larger amplifications of the CGG trinucleotide repeat of the FMR-1 gene. No physical differences were detectable in our study between fra(X) males with high expression and apparently larger amplifications of the CGG trinucleotide repeats compared with those patients with low expression. Our research illustrates the use of anthropometry in identifying differences between mentally retarded males with or without the fra(X) syndrome and offers a comprehensive approach for screening males for the fra(X) syndrome and selecting those individuals for cytogenetic and/or molecular genetic testing.
对34项身体参数制定了人体测量和颅面轮廓模式,该模式表明与总体均值的百分比差异。这些参数来自31名患有脆性X综合征(fra(X))的白人智障男性(23名成年人和8名儿童),他们在年龄上与31名病因不明的白人智障男性相匹配。患有fra(X)综合征的男性在所有人体测量变量上的尺寸始终较大,在身高、坐高、臂展、手长、中指长度、手宽、足长、足宽和睾丸体积方面存在显著差异。两组智障男性之间确实出现了颅面模式,但有几个变量存在重叠。在头围、头宽、面下高、颧间径、内眦距离、耳长和耳宽方面存在显著差异,患有fra(X)综合征的男性头部尺寸较大(头围、头宽、头长、面高和面下高),但最小额径、颧间径、下颌角径和内眦距离的测量值较小。在患有和未患有fra(X)综合征的智障男性的变量之间发现了几个显著的相关性。在一项对19个变量的人体测量和颅面轮廓综合研究中,比较了26名患有fra(X)综合征的白人男性(13名高表达(>30%)和13名低表达(<30%),但年龄匹配),观察到一个相对扁平的轮廓,任何变量之间均无显著差异。一般来说,脆性X染色体表达增加的fra(X)综合征男性,其FMR-1基因的CGG三核苷酸重复序列扩增更大。在我们的研究中,与低表达患者相比,高表达且CGG三核苷酸重复序列明显扩增的fra(X)男性之间未检测到身体差异。我们的研究说明了人体测量学在识别患有或未患有fra(X)综合征的智障男性之间差异方面的用途,并为筛查男性是否患有fra(X)综合征以及选择那些进行细胞遗传学和/或分子遗传学检测的个体提供了一种全面的方法。