Saksena S S, Bixler D
Department of Oral-Facial Genetics, I.U. Medical Center, Indianapolis, Indiana 46202.
Am J Med Genet. 1990 Jan;35(1):105-14. doi: 10.1002/ajmg.1320350120.
Roentgenographic measurements and morphometric analysis were employed in the investigation of contrasting patterns of craniofacial variation between normal individuals and those affected by X-linked hypohidrotic ectodermal dysplasia (HED). The research objective was to identify and describe the facial characteristics of heterozygous gene carriers who show minor expression of the disorder. In this study of 13 HED families with 16 affected males, 12 carriers, and 12 normal individuals, affected individuals had at least 3 of the following 4 clinical signs and symptoms: a) hypodontia, b) hypohidrosis, c) hypotrichosis, and d) clinically distinct facial physiognomy. By contrast, the gene carriers manifested only one or 2 or none of the 4 clinical manifestations. In a preliminary comparison of gene carriers vs. normal individuals, we have generated 2 discriminant functions (each based on 3 facial measurements taken either from the lateral or frontal cephalograms). These 2 functions correctly diagnose 100% of the gene carriers and normal HED relatives. Facial anomalies characteristic of the gene carriers were 1) abnormally narrow and short maxillary width and palatal depth dimensions; 2) very small and retrusive malar and maxillary regions; 3) markedly reduced lower facial depth, height and width dimensions; 4) small head height, prominent forehead, and high-set orbits; 5) a generalized, symmetric reduction of the whole craniofacial complex.
采用X线测量和形态计量分析,研究正常个体与X连锁低汗性外胚层发育不良(HED)患者颅面变异的对比模式。研究目的是识别和描述表现出该疾病轻微症状的杂合基因携带者的面部特征。在这项对13个HED家族的研究中,有16名患病男性、12名携带者和12名正常个体,患病个体至少有以下4种临床体征和症状中的3种:a)牙发育不全,b)少汗,c)毛发稀少,d)临床上明显不同的面部容貌。相比之下,基因携带者仅表现出这4种临床表现中的1种、2种或没有。在基因携带者与正常个体的初步比较中,我们生成了2个判别函数(每个函数基于从侧位或正位头颅X线片获取的3项面部测量数据)。这2个函数能正确诊断出100%的基因携带者和正常的HED亲属。基因携带者特有的面部异常包括:1)上颌宽度和腭深度维度异常狭窄和短小;2)颧骨和上颌区域非常小且后缩;3)面下部深度、高度和宽度维度明显减小;4)头高小、前额突出和眶位高;5)整个颅面部复合体普遍对称缩小。