Literature DB >> 31138847

Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan.

Hiroyuki Mishima1, Hisato Suzuki2, Michiko Doi3, Mutsuko Miyazaki4, Satoshi Watanabe5, Tadashi Matsumoto6, Kanako Morifuji7, Hiroyuki Moriuchi5, Koh-Ichiro Yoshiura8, Tatsuro Kondoh6, Kenjiro Kosaki2.   

Abstract

An increasing number of genetic syndromes present a challenge to clinical geneticists. A deep learning-based diagnosis assistance system, Face2Gene, utilizes the aggregation of "gestalt," comprising data summarizing features of patients' facial images, to suggest candidate syndromes. Because Face2Gene's results may be affected by ethnicity and age at which training facial images were taken, the system performance for patients in Japan is still unclear. Here, we present an evaluation of Face2Gene using the following two patient groups recruited in Japan: Group 1 consisting of 74 patients with 47 congenital dysmorphic syndromes, and Group 2 consisting of 34 patients with Down syndrome. In Group 1, facial recognition failed for 4 of 74 patients, while 13-21 of 70 patients had a diagnosis for which Face2Gene had not been trained. Omitting these 21 patients, for 85.7% (42/49) of the remainder, the correct syndrome was identified within the top 10 suggested list. In Group 2, for the youngest facial images taken for each of the 34 patients, Down syndrome was successfully identified as the highest-ranking condition using images taken from newborns to those aged 25 years. For the oldest facial images taken at ≥20 years in each of 17 applicable patients, Down syndrome was successfully identified as the highest- and second-highest-ranking condition in 82.2% (14/17) and 100% (17/17) of the patients using images taken from 20 to 40 years. These results suggest that Face2Gene in its current format is already useful in suggesting candidate syndromes to clinical geneticists, using patients with congenital dysmorphic syndromes in Japan.

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Year:  2019        PMID: 31138847     DOI: 10.1038/s10038-019-0619-z

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  18 in total

1.  Patients with SATB2-associated syndrome exhibiting multiple odontomas.

Authors:  Takashi Kikuiri; Hiroyuki Mishima; Hideto Imura; Satoshi Suzuki; Yusuke Matsuzawa; Takashi Nakamura; Satoshi Fukumoto; Yoshitaka Yoshimura; Satoshi Watanabe; Akira Kinoshita; Takahiro Yamada; Masanobu Shindoh; Yoshihiko Sugita; Hatsuhiko Maeda; Yasutaka Yawaka; Tadashi Mikoya; Nagato Natsume; Koh-Ichiro Yoshiura
Journal:  Am J Med Genet A       Date:  2018-12-21       Impact factor: 2.802

2.  Computer-Aided Recognition of Facial Attributes for Fetal Alcohol Spectrum Disorders.

Authors:  Matthew Valentine; Dustin C J Bihm; Lior Wolf; H Eugene Hoyme; Philip A May; David Buckley; Wendy Kalberg; Omar A Abdul-Rahman
Journal:  Pediatrics       Date:  2017-12       Impact factor: 7.124

3.  Next generation phenotyping in Emanuel and Pallister-Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos.

Authors:  T Liehr; N Acquarola; K Pyle; S St-Pierre; M Rinholm; O Bar; K Wilhelm; I Schreyer
Journal:  Clin Genet       Date:  2017-11-29       Impact factor: 4.438

4.  Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome.

Authors:  Yuri A Zarate; Constance L Smith-Hicks; Carol Greene; Mary-Alice Abbott; Victoria M Siu; Amy R U L Calhoun; Arti Pandya; Chumei Li; Elizabeth A Sellars; Julie Kaylor; Katherine Bosanko; Louisa Kalsner; Alice Basinger; Anne M Slavotinek; Hazel Perry; Margarita Saenz; Marta Szybowska; Louise C Wilson; Ajith Kumar; Caroline Brain; Meena Balasubramanian; Holly Dubbs; Xilma R Ortiz-Gonzalez; Elaine Zackai; Quinn Stein; Cynthia M Powell; Samantha Schrier Vergano; Allison Britt; Angela Sun; Wendy Smith; E Martina Bebin; Jonathan Picker; Amelia Kirby; Hailey Pinz; Hannah Bombei; Sonal Mahida; Julie S Cohen; Ali Fatemi; Hilary J Vernon; Rebecca McClellan; Leah R Fleming; Brittney Knyszek; Michelle Steinraths; Cruz Velasco Gonzalez; Anita E Beck; Katie L Golden-Grant; Alena Egense; Aditi Parikh; Chantalle Raimondi; Brad Angle; William Allen; Suzanna Schott; Adi Algrabli; Nathaniel H Robin; Joseph W Ray; David B Everman; Michael J Gambello; Wendy K Chung
Journal:  Am J Med Genet A       Date:  2018-02-13       Impact factor: 2.802

5.  From gestalt to gene: early predictive dysmorphic features of PMM2-CDG.

Authors:  Antonio Martinez-Monseny; Daniel Cuadras; Mercè Bolasell; Jordi Muchart; César Arjona; Mar Borregan; Adi Algrabli; Raquel Montero; Rafael Artuch; Ramón Velázquez-Fragua; Alfons Macaya; Celia Pérez-Cerdá; Belén Pérez-Dueñas; Belén Pérez; Mercedes Serrano
Journal:  J Med Genet       Date:  2018-11-21       Impact factor: 6.318

6.  The role of objective facial analysis using FDNA in making diagnoses following whole exome analysis. Report of two patients with mutations in the BAF complex genes.

Authors:  Karen W Gripp; Laura Baker; Aida Telegrafi; Kristin G Monaghan
Journal:  Am J Med Genet A       Date:  2016-04-26       Impact factor: 2.802

7.  Further delineation of Aymé-Gripp syndrome and use of automated facial analysis tool.

Authors:  Shivarajan M Amudhavalli; Randi Hanson; Brad Angle; Kelly Bontempo; Karen W Gripp
Journal:  Am J Med Genet A       Date:  2018-07       Impact factor: 2.802

8.  Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis.

Authors:  Alexej Knaus; Jean Tori Pantel; Manuela Pendziwiat; Nurulhuda Hajjir; Max Zhao; Tzung-Chien Hsieh; Max Schubach; Yaron Gurovich; Nicole Fleischer; Marten Jäger; Sebastian Köhler; Hiltrud Muhle; Christian Korff; Rikke S Møller; Allan Bayat; Patrick Calvas; Nicolas Chassaing; Hannah Warren; Steven Skinner; Raymond Louie; Christina Evers; Marc Bohn; Hans-Jürgen Christen; Myrthe van den Born; Ewa Obersztyn; Agnieszka Charzewska; Milda Endziniene; Fanny Kortüm; Natasha Brown; Peter N Robinson; Helenius J Schelhaas; Yvonne Weber; Ingo Helbig; Stefan Mundlos; Denise Horn; Peter M Krawitz
Journal:  Genome Med       Date:  2018-01-09       Impact factor: 11.117

9.  Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism.

Authors:  Jean T Pantel; Max Zhao; Martin A Mensah; Nurulhuda Hajjir; Tzung-Chien Hsieh; Yair Hanani; Nicole Fleischer; Tom Kamphans; Stefan Mundlos; Yaron Gurovich; Peter M Krawitz
Journal:  J Inherit Metab Dis       Date:  2018-04-05       Impact factor: 4.982

10.  Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders.

Authors:  Douglas R Stewart; Alexander Pemov; Jennifer J Johnston; Julie C Sapp; Meredith Yeager; Ji He; Joseph F Boland; Laurie Burdett; Christina Brown; Richard A Gatti; Blanche P Alter; Leslie G Biesecker; Sharon A Savage
Journal:  PLoS One       Date:  2014-06-03       Impact factor: 3.240

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  15 in total

1.  Differentiation of MISSLA and Fanconi anaemia by computer-aided image analysis and presentation of two novel MISSLA siblings.

Authors:  Magdalena Danyel; Zhuo Cheng; Christine Jung; Felix Boschann; Jean Tori Pantel; Nurulhuda Hajjir; Ricarda Flöttmann; Solveig Schulz; Ilja Demuth; Eamonn Sheridan; Stefan Mundlos; Denise Horn; Martin A Mensah
Journal:  Eur J Hum Genet       Date:  2019-07-18       Impact factor: 4.246

2.  Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience.

Authors:  Muhsin Elmas; Basak Gogus
Journal:  Mol Syndromol       Date:  2020-02-01

Review 3.  [Telemedical applications in ophthalmology in times of COVID-19].

Authors:  Lars Choritz; Michael Hoffmann; Hagen Thieme
Journal:  Ophthalmologe       Date:  2021-08-18       Impact factor: 1.059

4.  Application of Machine Learning in Translational Medicine: Current Status and Future Opportunities.

Authors:  Nadia Terranova; Karthik Venkatakrishnan; Lisa J Benincosa
Journal:  AAPS J       Date:  2021-05-18       Impact factor: 4.009

5.  Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes.

Authors:  Ana Latorre-Pellicer; Ángela Ascaso; Laura Trujillano; Marta Gil-Salvador; Maria Arnedo; Cristina Lucia-Campos; Rebeca Antoñanzas-Pérez; Iñigo Marcos-Alcalde; Ilaria Parenti; Gloria Bueno-Lozano; Antonio Musio; Beatriz Puisac; Frank J Kaiser; Feliciano J Ramos; Paulino Gómez-Puertas; Juan Pié
Journal:  Int J Mol Sci       Date:  2020-02-04       Impact factor: 5.923

Review 6.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

7.  Diagnostic performance of artificial intelligence to detect genetic diseases with facial phenotypes: A protocol for systematic review and meta analysis.

Authors:  Bosheng Qin; Qiyao Quan; Jingchao Wu; Letian Liang; Dongxiao Li
Journal:  Medicine (Baltimore)       Date:  2020-07-02       Impact factor: 1.817

8.  Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study.

Authors:  Jean Tori Pantel; Nurulhuda Hajjir; Magdalena Danyel; Jonas Elsner; Angela Teresa Abad-Perez; Peter Hansen; Stefan Mundlos; Malte Spielmann; Denise Horn; Claus-Eric Ott; Martin Atta Mensah
Journal:  J Med Internet Res       Date:  2020-10-22       Impact factor: 5.428

9.  Assessment of Facial Morphologic Features in Patients With Congenital Adrenal Hyperplasia Using Deep Learning.

Authors:  Wael AbdAlmageed; Hengameh Mirzaalian; Xiao Guo; Linda M Randolph; Veeraya K Tanawattanacharoen; Mitchell E Geffner; Heather M Ross; Mimi S Kim
Journal:  JAMA Netw Open       Date:  2020-11-02

10.  A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family.

Authors:  Afrooz Sepahvand; Ehsan Razmara; Fatemeh Bitarafan; Mohammad Galehdari; Ali Reza Tavasoli; Navid Almadani; Masoud Garshasbi
Journal:  Mol Genet Genomic Med       Date:  2020-07-22       Impact factor: 2.183

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