Literature DB >> 16773127

Syndrome identification based on 2D analysis software.

Stefan Boehringer1, Tobias Vollmar, Christiane Tasse, Rolf P Wurtz, Gabriele Gillessen-Kaesbach, Bernhard Horsthemke, Dagmar Wieczorek.   

Abstract

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.

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Year:  2006        PMID: 16773127     DOI: 10.1038/sj.ejhg.5201673

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  19 in total

1.  Shape-based classification of 3D facial data to support 22q11.2DS craniofacial research.

Authors:  Katarzyna Wilamowska; Jia Wu; Carrie Heike; Linda Shapiro
Journal:  J Digit Imaging       Date:  2012-06       Impact factor: 4.056

2.  Down syndrome diagnosis based on Gabor Wavelet Transform.

Authors:  Safak Saraydemir; Necmi Taşpınar; Osman Eroğul; Hülya Kayserili; Nuriye Dinçkan
Journal:  J Med Syst       Date:  2011-11-30       Impact factor: 4.460

Review 3.  The use of 3D face shape modelling in dysmorphology.

Authors: 
Journal:  Arch Dis Child       Date:  2007-12       Impact factor: 3.791

4.  A Dysmorphometric Analysis to Investigate Facial Phenotypic Signatures as a Foundation for Non-invasive Monitoring of Lysosomal Storage Disorders.

Authors:  Stefanie Kung; Mark Walters; Peter Claes; Jack Goldblatt; Peter Le Souef; Gareth Baynam
Journal:  JIMD Rep       Date:  2012-06-10

5.  De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism.

Authors:  Illja J Diets; Roos van der Donk; Kristina Baltrunaite; Esmé Waanders; Margot R F Reijnders; Alexander J M Dingemans; Rolph Pfundt; Anneke T Vulto-van Silfhout; Laurens Wiel; Christian Gilissen; Julien Thevenon; Laurence Perrin; Alexandra Afenjar; Caroline Nava; Boris Keren; Sarah Bartz; Bethany Peri; Gea Beunders; Nienke Verbeek; Koen van Gassen; Isabelle Thiffault; Maxime Cadieux-Dion; Lina Huerta-Saenz; Matias Wagner; Vassiliki Konstantopoulou; Julia Vodopiutz; Matthias Griese; Annekatrien Boel; Bert Callewaert; Han G Brunner; Tjitske Kleefstra; Nicoline Hoogerbrugge; Bert B A de Vries; Vivian Hwa; Andrew Dauber; Jayne Y Hehir-Kwa; Roland P Kuiper; Marjolijn C J Jongmans
Journal:  Am J Hum Genet       Date:  2019-03-28       Impact factor: 11.025

6.  Down syndrome detection based on facial features using a geometric descriptor.

Authors:  Jadisha Yarif Ramírez Cornejo; Helio Pedrini; Ariane Machado-Lima; Fátima de Lourdes Dos Santos Nunes
Journal:  J Med Imaging (Bellingham)       Date:  2017-12-12

7.  Genetic determination of human facial morphology: links between cleft-lips and normal variation.

Authors:  Stefan Boehringer; Fedde van der Lijn; Fan Liu; Manuel Günther; Stella Sinigerova; Stefanie Nowak; Kerstin U Ludwig; Ruth Herberz; Stefan Klein; Albert Hofman; Andre G Uitterlinden; Wiro J Niessen; Monique M B Breteler; Aad van der Lugt; Rolf P Würtz; Markus M Nöthen; Bernhard Horsthemke; Dagmar Wieczorek; Elisabeth Mangold; Manfred Kayser
Journal:  Eur J Hum Genet       Date:  2011-06-22       Impact factor: 4.246

8.  Shape-Based Classification of 3D Head Data.

Authors:  Linda Shapiro; Katarzyna Wilamowska; Indriyati Atmosukarto; Jia Wu; Carrie Heike; Matthew Speltz; Michael Cunningham
Journal:  Proc Int Conf Image Anal Process       Date:  2009

9.  Craniofacial characteristics of fragile X syndrome in mouse and man.

Authors:  Inge Heulens; Michael Suttie; Andrei Postnov; Nora De Clerck; Concetta S Perrotta; Teresa Mattina; Francesca Faravelli; Francesca Forzano; R Frank Kooy; Peter Hammond
Journal:  Eur J Hum Genet       Date:  2012-12-05       Impact factor: 4.246

10.  The Use of Genetic Programming for Learning 3D Craniofacial Shape Quantifications.

Authors:  Indriyati Atmosukarto; Linda G Shapiro; Carrie Heike
Journal:  Proc IAPR Int Conf Pattern Recogn       Date:  2010
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