Literature DB >> 27925162

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.

A Lumaka1,2,3,4, N Cosemans1, A Lulebo Mampasi5, G Mubungu2,3, N Mvuama5, T Lubala6, S Mbuyi-Musanzayi6, J Breckpot1, M Holvoet1, T de Ravel1, G Van Buggenhout1, H Peeters1, D Donnai7, L Mutesa8, A Verloes9, P Lukusa Tshilobo1,2,3,4, K Devriendt1.   

Abstract

The evaluation of facial dysmorphism is a critical step toward reaching a diagnostic. The aim of the present study was to evaluate the ability to interpret facial morphology in African children with intellectual disability (ID). First, 10 experienced clinicians (five from Africa and five from Europe) rated gestalt in 127 African non-Down Syndrome (non-DS) patients using either the score 2 for 'clearly dysmorphic', 0 for 'clearly non dysmorphic' or 1 for 'uncertain'. The inter-rater agreement was determined using kappa coefficient. There was only fair agreement between African and European raters (kappa-coefficient = 0.29). Second, we applied the FDNA Face2Gene solution to assess Down Syndrome (DS) faces. Initially, Face2Gene showed a better recognition rate for DS in Caucasian (80%) compared to African (36.8%). We trained the Face2Gene with a set of African DS and non-DS photographs. Interestingly, the recognition in African increased to 94.7%. Thus, training improved the sensitivity of Face2Gene. Our data suggest that human based evaluation is influenced by ethnic background of the evaluator. In addition, computer based evaluation indicates that the ethnic of the patient also influences the evaluation and that training may increase the detection specificity for a particular ethnic.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  DR Congo; Down syndrome; Face2Gene; dysmorphology; facial dysmorphism; gestalt

Mesh:

Year:  2017        PMID: 27925162     DOI: 10.1111/cge.12948

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  17 in total

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

Authors:  Hiroyuki Mishima; Hisato Suzuki; Michiko Doi; Mutsuko Miyazaki; Satoshi Watanabe; Tadashi Matsumoto; Kanako Morifuji; Hiroyuki Moriuchi; Koh-Ichiro Yoshiura; Tatsuro Kondoh; Kenjiro Kosaki
Journal:  J Hum Genet       Date:  2019-05-29       Impact factor: 3.172

Review 2.  Recognizable phenotypes in CDG.

Authors:  Carlos R Ferreira; Ruqaia Altassan; Dorinda Marques-Da-Silva; Rita Francisco; Jaak Jaeken; Eva Morava
Journal:  J Inherit Metab Dis       Date:  2018-04-13       Impact factor: 4.982

3.  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

4.  The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiers.

Authors:  Giulia Pascolini; Nicole Fleischer; Alessandro Ferraris; Silvia Majore; Paola Grammatico
Journal:  J Hum Genet       Date:  2019-05-13       Impact factor: 3.172

5.  Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa.

Authors:  Sébastien Mbuyi-Musanzayi; Aimé Lumaka; Toni Lubala Kasole; Erick Kasamba Ilunga; Bienvenu Yogolelo Asani; Prosper Lukusa Tshilobo; Prosper Kalenga Muenze; Hervé Reychler; François Tshilombo Katombe; Koenraad Devriendt
Journal:  J Pediatr Genet       Date:  2017-03-07

6.  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

7.  Cerebro-facio-thoracic dysplasia (Pascual-Castroviejo syndrome): Identification of a novel mutation, use of facial recognition analysis, and review of the literature.

Authors:  Jennifer A F Tender; Carlos R Ferreira
Journal:  Transl Sci Rare Dis       Date:  2018-04-13

8.  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

9.  Fragile X checklists: A meta-analysis and development of a simplified universal clinical checklist.

Authors:  Toni Kasole Lubala; Aimé Lumaka; Gray Kanteng; Léon Mutesa; Olivier Mukuku; Stanislas Wembonyama; Randi Hagerman; Oscar Numbi Luboya; Prosper Lukusa Tshilobo
Journal:  Mol Genet Genomic Med       Date:  2018-04-06       Impact factor: 2.183

Review 10.  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

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