Schaumann B A, Kimura S
Veterans Affairs Medical Center, Portland, OR.
Birth Defects Orig Artic Ser. 1991;27(2):229-52.
The above overview illustrates the areas of interest in flexion creases in human biology studies in general and in studies of medical disorders in particular. Clearly, flexion creases have a significance of their own rather than only as appendices of the dermatoglyphic analysis and should, therefore, be approached appropriately. In some instances, they may be of more interest than the dermatoglyphics. Our understanding of the creases and their value is, however, as yet incomplete and the gaps in our insight limit the possible interpretations and practical applications of the knowledge gained from studies of various aspects of the flexion creases. Creases provide important clues of the early fetal development and thus may be of practical value in clinical medicine. So far, most of these studies have been carried out in relation to specific disorders, often without a clear reasoning why flexion creases should be altered in the given disorder. The examples of aberrant flexion creases discussed above illustrate the general lack of specificity of crease anomalies in association with a particular syndrome or disorder that does not include malformations or malfunctions of the limbs. Instead, the anomalous flexion creases reflect the altered shape and function of hand and foot, which, in turn, are determined during early fetal development and affected by factors interfering with normal embryogenesis. A more promising approach to studying flexion creases in medical disorders, therefore, is to explore the developmental correlations between the creases and the structure and function of hands and feet. This does not mean that information gained from the case reports of individuals with various congenital defects is of no value. On the contrary, it should be collected systematically to determine the variety of crease aberrations and their frequencies in a given disorder, which would help elucidate the presence and timing of the developmental factors involved in the origin of the defect. The usefulness and limitations of the flexion creases are to a large degree parallel to those of dermatoglyphics. Altered flexion creases are indicative of intrauterine disturbances occurring early in pregnancy. As such, they may be of a predictive value in otherwise apparently normal infants in whom cryptic damage may be manifested later. They may serve to alert the physician to perform careful or more detailed examinations or to reexamine already obtained (and possibly inaccurate) test results. A better understanding of the crease embryology, both normal and abnormal, is a prerequisite for progress in studies of flexion creases.(ABSTRACT TRUNCATED AT 400 WORDS)
上述概述阐述了人类生物学研究中,尤其是医学疾病研究中对屈褶纹感兴趣的领域。显然,屈褶纹有其自身的重要性,而非仅仅作为皮纹分析的附属部分,因此应予以恰当研究。在某些情况下,它们可能比皮纹更具研究价值。然而,我们对屈褶纹及其价值的理解尚不完整,认知上的差距限制了从屈褶纹各方面研究中获取的知识的可能解读和实际应用。屈褶纹为胎儿早期发育提供了重要线索,因而在临床医学中可能具有实用价值。到目前为止,大多数此类研究是针对特定疾病进行的,往往没有明确的理由解释为何在特定疾病中屈褶纹会发生改变。上述异常屈褶纹的例子表明,与不包括肢体畸形或功能障碍的特定综合征或疾病相关的屈褶纹异常普遍缺乏特异性。相反,异常屈褶纹反映了手和脚的形态及功能的改变,而手和脚的形态及功能又在胎儿早期发育过程中确定,并受干扰正常胚胎发生的因素影响。因此,在医学疾病中研究屈褶纹的一种更有前景的方法是探索屈褶纹与手和脚的结构及功能之间的发育相关性。这并不意味着从患有各种先天性缺陷个体的病例报告中获得的信息毫无价值。相反,应系统收集这些信息,以确定特定疾病中屈褶纹异常的种类及其出现频率,这将有助于阐明缺陷起源中涉及的发育因素的存在及时间。屈褶纹的有用性和局限性在很大程度上与皮纹相似。改变的屈褶纹表明妊娠早期发生了子宫内干扰。因此,它们可能对其他看似正常但可能在后期出现隐匿性损伤迹象的婴儿具有预测价值。它们可能促使医生进行仔细或更详细的检查,或重新检查已获得的(可能不准确的)检测结果。更好地理解正常和异常的屈褶纹胚胎学是屈褶纹研究取得进展 的前提条件。(摘要截选至400字)