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Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan.
Mishima, Hiroyuki; Suzuki, Hisato; Doi, Michiko; Miyazaki, Mutsuko; Watanabe, Satoshi; Matsumoto, Tadashi; Morifuji, Kanako; Moriuchi, Hiroyuki; Yoshiura, Koh-Ichiro; Kondoh, Tatsuro; Kosaki, Kenjiro.
Afiliación
  • Mishima H; Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. hmishima@nagasaki-u.ac.jp.
  • Suzuki H; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Doi M; Department of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan.
  • Miyazaki M; Department of Pediatrics, Nagasaki Prefectural Children Medical Welfare Center, Isahaya, Japan.
  • Watanabe S; Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Matsumoto T; Division of Developmental Disabilities, Misakaenosono Mutsumi Developmental, Medical and Welfare Center, Isahaya, Japan.
  • Morifuji K; Department of Nursing, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Moriuchi H; Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Yoshiura KI; Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Kondoh T; Division of Developmental Disabilities, Misakaenosono Mutsumi Developmental, Medical and Welfare Center, Isahaya, Japan.
  • Kosaki K; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
J Hum Genet ; 64(8): 789-794, 2019 Aug.
Article en En | MEDLINE | ID: mdl-31138847
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Diagnóstico por Imagen / Facies / Anomalías Craneofaciales / Identificación Biométrica Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Diagnóstico por Imagen / Facies / Anomalías Craneofaciales / Identificación Biométrica Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Japón