Literature DB >> 24579144

Hierarchical constrained local model using ICA and its application to Down syndrome detection.

Qian Zhao1, Kazunori Okada2, Kenneth Rosenbaum3, Dina J Zand3, Raymond Sze1, Marshall Summar3, Marius George Linguraru1.   

Abstract

Conventional statistical shape models use Principal Component Analysis (PCA) to describe shape variations. However, such a PCA-based model assumes a Gaussian distribution of data. A model with Independent Component Analysis (ICA) does not require the Gaussian assumption and can additionally describe the local shape variation. In this paper, we propose a Hierarchical Constrained Local Model (HCLM) using ICA. The first or coarse level of HCLM locates the full landmark set, while the second level refines a relevant landmark subset. We then apply the HCLM to Down syndrome detection from photographs of young pediatric patients. Down syndrome is the most common chromosomal condition and its early detection is crucial. After locating facial anatomical landmarks using HCLM, geometric and local texture features are extracted and selected. A variety of classifiers are evaluated to identify Down syndrome from a healthy population. The best performance achieved 95.6% accuracy using support vector machine with radial basis function kernel. The results show that the ICA-based HCLM outperformed both PCA-based CLM and ICA-based CLM.

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Year:  2013        PMID: 24579144     DOI: 10.1007/978-3-642-40763-5_28

Source DB:  PubMed          Journal:  Med Image Comput Comput Assist Interv


  9 in total

1.  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

2.  Cornelia de Lange syndrome in diverse populations.

Authors:  Leah Dowsett; Antonio R Porras; Paul Kruszka; Brandon Davis; Tommy Hu; Engela Honey; Eben Badoe; Meow-Keong Thong; Eyby Leon; Katta M Girisha; Anju Shukla; Shalini S Nayak; Vorasuk Shotelersuk; Andre Megarbane; Shubha Phadke; Nirmala D Sirisena; Vajira H W Dissanayake; Carlos R Ferreira; Monisha S Kisling; Pranoot Tanpaiboon; Annette Uwineza; Leon Mutesa; Cedrik Tekendo-Ngongang; Ambroise Wonkam; Karen Fieggen; Leticia Cassimiro Batista; Danilo Moretti-Ferreira; Roger E Stevenson; Eloise J Prijoles; David Everman; Kate Clarkson; Jessica Worthington; Virginia Kimonis; Fuki Hisama; Carol Crowe; Paul Wong; Kisha Johnson; Robin D Clark; Lynne Bird; Diane Masser-Frye; Marie McDonald; Patrick Willems; Elizabeth Roeder; Sulgana Saitta; Kwame Anyane-Yeoba; Laurie Demmer; Naoki Hamajima; Zornitza Stark; Greta Gillies; Louanne Hudgins; Usha Dave; Stavit Shalev; Victoria Siu; Ann Ades; Holly Dubbs; Sarah Raible; Maninder Kaur; Emanuela Salzano; Laird Jackson; Matthew Deardorff; Antonie Kline; Marshall Summar; Maximilian Muenke; Marius George Linguraru; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2019-01-06       Impact factor: 2.802

3.  22q11.2 deletion syndrome in diverse populations.

Authors:  Paul Kruszka; Yonit A Addissie; Daniel E McGinn; Antonio R Porras; Elijah Biggs; Matthew Share; T Blaine Crowley; Brian H Y Chung; Gary T K Mok; Christopher C Y Mak; Premala Muthukumarasamy; Meow-Keong Thong; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; L B Lahiru Prabodha; Rupesh Mishra; Vorasuk Shotelersuk; Ekanem Nsikak Ekure; Ogochukwu Jidechukwu Sokunbi; Nnenna Kalu; Carlos R Ferreira; Jordann-Mishael Duncan; Siddaramappa Jagdish Patil; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Annette Uwineza; Leon Mutesa; Angélica Moresco; María Gabriela Obregon; Antonio Richieri-Costa; Vera L Gil-da-Silva-Lopes; Adebowale A Adeyemo; Marshall Summar; Elaine H Zackai; Donna M McDonald-McGinn; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2017-04       Impact factor: 2.802

4.  Noonan syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Yonit A Addissie; Angélica Moresco; Sofia Medrano; Gary T K Mok; Gordon K C Leung; Cedrik Tekendo-Ngongang; Annette Uwineza; Meow-Keong Thong; Premala Muthukumarasamy; Engela Honey; Ekanem N Ekure; Ogochukwu J Sokunbi; Nnenna Kalu; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Lisa M Vincent; Amber Love; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Anju Shukla; Katta M Girisha; Siddaramappa J Patil; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Eva Klein-Zighelboim; Bertha E Gallardo Jugo; Miguel Chávez Pastor; Hugo H Abarca-Barriga; Steven A Skinner; Eloise J Prijoles; Eben Badoe; Ashleigh D Gill; Vorasuk Shotelersuk; Patroula Smpokou; Monisha S Kisling; Carlos R Ferreira; Leon Mutesa; Andre Megarbane; Antonie D Kline; Amy Kimball; Emmy Okello; Peter Lwabi; Twalib Aliku; Emmanuel Tenywa; Nonglak Boonchooduang; Pranoot Tanpaiboon; Antonio Richieri-Costa; Ambroise Wonkam; Brian H Y Chung; Roger E Stevenson; Marshall Summar; Kausik Mandal; Shubha R Phadke; María G Obregon; Marius G Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2017-07-27       Impact factor: 2.802

5.  Facial analysis technology for the detection of Down syndrome in the Democratic Republic of the Congo.

Authors:  Antonio R Porras; Matthew S Bramble; Kizito Mosema Be Amoti; D'Andre Spencer; Cécile Dakande; Hans Manya; Neerja Vashist; Esther Likuba; Joachim Mukau Ebwel; Céleste Musasa; Helen Malherbe; Bilal Mohammed; Carlos Tor-Diez; Dieudonné Mumba Ngoyi; Désiré Tshala Katumbay; Marius George Linguraru; Eric Vilain
Journal:  Eur J Med Genet       Date:  2021-06-20       Impact factor: 2.465

6.  Williams-Beuren syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Deise Helena de Souza; Angélica Moresco; Victoria Huckstadt; Ashleigh D Gill; Alec P Boyle; Tommy Hu; Yonit A Addissie; Gary T K Mok; Cedrik Tekendo-Ngongang; Karen Fieggen; Eloise J Prijoles; Pranoot Tanpaiboon; Engela Honey; Ho-Ming Luk; Ivan F M Lo; Meow-Keong Thong; Premala Muthukumarasamy; Kelly L Jones; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Laila Bouguenouch; Anju Shukla; Katta M Girisha; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Monisha S Kisling; Carlos R Ferreira; María Beatriz de Herreros; Ni-Chung Lee; Saumya S Jamuar; Angeline Lai; Ee Shien Tan; Jiin Ying Lim; Cham Breana Wen-Min; Neerja Gupta; Stephanie Lotz-Esquivel; Ramsés Badilla-Porras; Dalia Farouk Hussen; Mona O El Ruby; Engy A Ashaat; Siddaramappa J Patil; Leah Dowsett; Alison Eaton; A Micheil Innes; Vorasuk Shotelersuk; Ëben Badoe; Ambroise Wonkam; María Gabriela Obregon; Brian H Y Chung; Milana Trubnykova; Jorge La Serna; Bertha Elena Gallardo Jugo; Miguel Chávez Pastor; Hugo Hernán Abarca Barriga; Andre Megarbane; Beth A Kozel; Mieke M van Haelst; Roger E Stevenson; Marshall Summar; A Adebowale Adeyemo; Colleen A Morris; Danilo Moretti-Ferreira; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.578

7.  A deep learning-based diagnostic tool for identifying various diseases via facial images.

Authors:  Omneya Attallah
Journal:  Digit Health       Date:  2022-09-10

8.  Bi-stream CNN Down Syndrome screening model based on genotyping array.

Authors:  Bing Feng; William Hoskins; Yan Zhang; Zibo Meng; David C Samuels; Jiandong Wang; Ruofan Xia; Chao Liu; Jijun Tang; Yan Guo
Journal:  BMC Med Genomics       Date:  2018-11-20       Impact factor: 3.063

Review 9.  Diagnosis support systems for rare diseases: a scoping review.

Authors:  Carole Faviez; Xiaoyi Chen; Nicolas Garcelon; Antoine Neuraz; Bertrand Knebelmann; Rémi Salomon; Stanislas Lyonnet; Sophie Saunier; Anita Burgun
Journal:  Orphanet J Rare Dis       Date:  2020-04-16       Impact factor: 4.123

  9 in total

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