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Facial analysis technology for the detection of Down syndrome in the Democratic Republic of the Congo.
Porras, Antonio R; Bramble, Matthew S; Mosema Be Amoti, Kizito; Spencer, D'Andre; Dakande, Cécile; Manya, Hans; Vashist, Neerja; Likuba, Esther; Ebwel, Joachim Mukau; Musasa, Céleste; Malherbe, Helen; Mohammed, Bilal; Tor-Diez, Carlos; Ngoyi, Dieudonné Mumba; Katumbay, Désiré Tshala; Linguraru, Marius George; Vilain, Eric.
Afiliação
  • Porras AR; Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA; Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. Electronic address: antonio.porras@cuanschutz.e
  • Bramble MS; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA.
  • Mosema Be Amoti K; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Biamba Marie Mutombo Hospital, Kinshasa, Democratic Republic of the Congo; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
  • Spencer D; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA.
  • Dakande C; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
  • Manya H; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
  • Vashist N; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Department of Genomics and Precision Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
  • Likuba E; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo.
  • Ebwel JM; Université Pédagogique Nationale, Kinshasa, Democratic Republic of the Congo.
  • Musasa C; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; Faculty of Medicine, Congo Protestant University, Kinshasa, Université Protestante au Congo.
  • Malherbe H; University of KwaZulu Natal, Durban, South Africa.
  • Mohammed B; Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA.
  • Tor-Diez C; Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA.
  • Ngoyi DM; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo; Department of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
  • Katumbay DT; Institut National de Recherche Biomédicale (INRB), Kinshasa, Democratic Republic of the Congo; Department of Neurology and School of Public Health, Oregon Health & Science University, Portland, OR, USA.
  • Linguraru MG; Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA; Departments of Radiology Pediatrics and Biomedical Engineering, George Washington University, Washington, DC, USA. Electronic address: mlingura@childrensnational.org.
  • Vilain E; Center for Genetic Medicine Research, Children's Research Institute, Children's National Hospital, Washington, DC, USA; International Research Laboratory of Epigenetics, Data, Politics, Centre National de la Recherche Scientifique, Washington, DC, USA; Department of Genomics and Precision Medicine,
Eur J Med Genet ; 64(9): 104267, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34161860
ABSTRACT
Down syndrome is one of the most common chromosomal anomalies affecting the world's population, with an estimated frequency of 1 in 700 live births. Despite its relatively high prevalence, diagnostic rates based on clinical features have remained under 70% for most of the developed world and even lower in countries with limited resources. While genetic and cytogenetic confirmation greatly increases the diagnostic rate, such resources are often non-existent in many low- and middle-income countries, particularly in Sub-Saharan Africa. To address the needs of countries with limited resources, the implementation of mobile, user-friendly and affordable technologies that aid in diagnosis would greatly increase the odds of success for a child born with a genetic condition. Given that the Democratic Republic of the Congo is estimated to have one of the highest rates of birth defects in the world, our team sought to determine if smartphone-based facial analysis technology could accurately detect Down syndrome in individuals of Congolese descent. Prior to technology training, we confirmed the presence of trisomy 21 using low-cost genomic applications that do not need advanced expertise to utilize and are available in many low-resourced countries. Our software technology trained on 132 Congolese subjects had a significantly improved performance (91.67% accuracy, 95.45% sensitivity, 87.88% specificity) when compared to previous technology trained on individuals who are not of Congolese origin (p < 5%). In addition, we provide the list of most discriminative facial features of Down syndrome and their ranges in the Congolese population. Collectively, our technology provides low-cost and accurate diagnosis of Down syndrome in the local population.
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Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Síndrome de Down / Fácies / Reconhecimento Facial Automatizado Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Síndrome de Down / Fácies / Reconhecimento Facial Automatizado Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Africa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article