Facial Expressiveness in Infants With and Without Craniofacial Microsomia.

Objective: To compare facial expressiveness (FE) of infants with and without craniofacial macrosomia (cases and controls, respectively) and to compare phenotypic variation among cases in relation to FE. Design: Positive and negative affect was elicited in response to standardized emotion inductions,...

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Publicado en:Cleft Palate Craniofacial Journal Vol. 55; no. 5; pp. 711 - 721
Autores principales: Hammal, Zakia, Cohn, Jeffrey F., Wallace, Erin R., Heike, Carrie L., Birgfeld, Craig B., Oster, Harriet, Speltz, Matthew L.
Formato: pictorial research tables/charts Journal Article
Publicado: Sage Publications Inc. May2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: May2018
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      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        atl: Facial Expressiveness in Infants With and Without Craniofacial Microsomia.
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        au:
          Hammal, Zakia
          Cohn, Jeffrey F.
          Wallace, Erin R.
          Heike, Carrie L.
          Birgfeld, Craig B.
          Oster, Harriet
          Speltz, Matthew L.
        affil: Robotics Institute, Carnegie Mellon University, Pittsburgh, PA, USA
      sug:
        subj:
          Goldenhar Syndrome Psychosocial Factors
          Facial Expression In Infancy and Childhood
          Phenotype
          Human
          Exploratory Research
          Case Control Studies
          Emotions
          Videorecording
          Hospitals, Pediatric United States
          United States
          Confidence Intervals
          Infant
          Prevalence
          Affect
          Mandible Pathology
          Nervous System Diseases
          Effect Size
          Infant: 1-23 months
      ab: Objective: To compare facial expressiveness (FE) of infants with and without craniofacial macrosomia (cases and controls, respectively) and to compare phenotypic variation among cases in relation to FE. Design: Positive and negative affect was elicited in response to standardized emotion inductions, video recorded, and manually coded from video using the Facial Action Coding System for Infants and Young Children. Setting: Five craniofacial centers: Children’s Hospital of Los Angeles, Children’s Hospital of Philadelphia, Seattle Children’s Hospital, University of Illinois–Chicago, and University of North Carolina–Chapel Hill. Participants: Eighty ethnically diverse 12- to 14-month-old infants. Main Outcome Measures: FE was measured on a frame-by-frame basis as the sum of 9 observed facial action units (AUs) representative of positive and negative affect. Results: FE differed between conditions intended to elicit positive and negative affect (95% confidence interval = 0.09-0.66, P = .01). FE failed to differ between cases and controls (ES = –0.16 to –0.02, P = .47 to .92). Among cases, those with and without mandibular hypoplasia showed similar levels of FE (ES = –0.38 to 0.54, P = .10 to .66). Conclusions: FE varied between positive and negative affect, and cases and controls responded similarly. Null findings for case/control differences may be attributable to a lower than anticipated prevalence of nerve palsy among cases, the selection of AUs, or the use of manual coding. In future research, we will reexamine group differences using an automated, computer vision approach that can cover a broader range of facial movements and their dynamics.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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