Syndrome identification based on 2D analysis software

被引:63
作者
Boehringer, Stefan
Vollmar, Tobias
Tasse, Christiane
Wurtz, Rolf P.
Gillessen-Kaesbach, Gabriele
Horsthemke, Bernhard
Wieczorek, Dagmar
机构
[1] Univ Klinikum Essen, Inst Human Genet, Essen, Germany
[2] Ruhr Univ Bochum, Inst Neuroinformat, D-4630 Bochum, Germany
关键词
syndrome diagnosis; face; facial appearance; statistical discrimination; learning;
D O I
10.1038/sj.ejhg.5201673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Clinical evaluation of children with developmental delay continues to present a challenge to the clinicians. In many cases, the face provides important information to diagnose a condition. However, database support with respect to facial traits is limited at present. Computer-based analyses of 2D and 3D representations of faces have been developed, but it is unclear how well a larger number of conditions can be handled by such systems. We have therefore analysed 2D pictures of patients each being affected with one of 10 syndromes ( fragile X syndrome; Cornelia de Lange syndrome; Williams-Beuren syndrome; Prader-Willi syndrome; Mucopolysaccharidosis type III; Cri-du-chat syndrome; Smith-Lemli-Opitz syndrome; Sotos syndrome; Microdeletion 22q11.2; Noonan syndrome). We can show that a classification accuracy of > 75% can be achieved for a computer-based diagnosis among the 10 syndromes, which is about the same accuracy achieved for five syndromes in a previous study. Pairwise discrimination of syndromes ranges from 80 to 99%. Furthermore, we can demonstrate that the criteria used by the computer decisions match clinical observations in many cases. These findings indicate that computer-based picture analysis might be a helpful addition to existing database systems, which are meant to assist in syndrome diagnosis, especially as data acquisition is straightforward and involves off-the-shelf digital camera equipment.
引用
收藏
页码:1082 / 1089
页数:8
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