Assessment of soft tissue facial asymmetry in medically normal and syndrome-affected individuals by analysis of landmarks and measurements
- 21 June 2000
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 93 (2) , 143-154
- https://doi.org/10.1002/1096-8628(20000717)93:2<143::aid-ajmg12>3.0.co;2-q
Abstract
We investigated soft tissue facial asymmetry in normal and syndrome‐affected individuals ranging in age from 1 year to adulthood. The purposes of our study were to determine if facial asymmetry was greater in syndrome‐affected individuals than in normal individuals and, if true, to distinguish those measurements that could be used in routine screening to identify the presence of syndromes in uncertain patients and, lastly, to investigate the causes of measurement asymmetry at the level of the landmarks. The last purpose was possible because we used a stereophotogrammetric method with which the three‐dimensional (3D) landmark positions were obtained. In the statistically significantly different measurements, those from the right side were dominant, with one exception in each group, except normal males. In all groups the landmark analyses demonstrated the same trends, and while there was far less patterning in the 3D coordinates, these results were also consistent between the four groups. We compared the statistical findings of the 3D coordinates and measurements and found that there was no predictable relationship between significant findings in the landmarks and the measurements. In particular, we noted that statistical differences in measurements did not infer significant differences in the positions of the landmarks between the right and left sides of the face. Both the normal and syndrome‐affected groups appeared to be equally canalized and similarly affected by developmental noise: When the bilateral measurement differences of each syndrome‐affected subject were compared to the limits of normal asymmetry, less than 10% of the comparisons exceeded the norms. Am. J. Med. Genet. 93:143–154, 2000.Keywords
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