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Cognitive, Motor, and Language Development of Preschool Children With Craniofacial Microsomia.
Collett, Brent R; Wallace, Erin R; Kapp-Simon, Kathleen A; Johns, Alexis L; Drake, Amelia F; Heike, Carrie L; Kinter, Sara; Luquetti, Daniela V; Magee, Leanne; Norton, Susan; Sie, Kathleen; Speltz, Matthew L.
Afiliação
  • Collett BR; Department of Psychiatry and Behavioral Sciences, 7284University of Washington, Seattle, WA, USA.
  • Wallace ER; Center for Child Health, Behavior, and Development, Seattle Children's Research Institute, Seattle, WA, USA.
  • Kapp-Simon KA; Department of Surgery, University of Illinois at Chicago and 24183Shriners Hospitals for Children, Chicago, IL, USA.
  • Johns AL; Clinical Pediatrics, 5150Children's Hospital of Los Angeles, Los Angeles, CA, USA.
  • Drake AF; Department of Otolaryngology/Head and Neck Surgery, 2331University of North Carolina, Chapel Hill, NC, USA.
  • Heike CL; Division of Craniofacial Medicine, Department of Pediatrics, 7274Seattle Children's Hospital, Seattle, WA, USA.
  • Kinter S; Seattle Children's Craniofacial Center, Seattle, WA, USA.
  • Luquetti DV; Division of Craniofacial Medicine, Department of Pediatrics, 7274Seattle Children's Hospital, Seattle, WA, USA.
  • Magee L; Division of Plastic and Reconstructive Surgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Norton S; Department of Otolaryngology, 7284University of Washington, Seattle, WA, USA.
  • Sie K; Department of Otolaryngology, 7284University of Washington, Seattle, WA, USA.
  • Speltz ML; Department of Psychiatry and Behavioral Sciences, 7284University of Washington, Seattle, WA, USA.
Cleft Palate Craniofac J ; 58(9): 1169-1177, 2021 09.
Article em En | MEDLINE | ID: mdl-33322943
ABSTRACT

OBJECTIVE:

To examine neurodevelopment in preschool-aged children with craniofacial microsomia (CFM) relative to unaffected peers.

DESIGN:

Multisite, longitudinal cohort study.

SETTING:

Tertiary care centers in the United States.

PARTICIPANTS:

We included 92 children with CFM ("cases") through craniofacial centers and clinics. Seventy-six children without CFM (controls) were included from pediatric practices and community advertisements. This study reports on outcomes assessed when participants were an average age of 38.4 months (SD = 1.9). MAIN OUTCOME

MEASURES:

We assessed cognitive and motor skills using the Bayley Scales of Infant and Toddler Development, third edition (Bayley-III), and language function using subtests from the Clinical Evaluation of Language Fundamentals-Preschool, second edition (CELF-P2).

RESULTS:

Case-control differences were negligible for Bayley-III cognitive (effect sizes [ES] = -0.06, P = .72) and motor outcomes (ES = -0.19, P = .25). Cases scored lower than controls on most scales of the CELF-P2 (ES = -0.58 to -0.20, P = .01 to .26). Frequency counts for "developmental delay" (ie, one or more scores > 1 SD below the normative mean) were higher for cases (39%) than controls (15%); however, the adjusted odds ratio = 1.73 (P = 0.21) was not significant. Case-control differences were most evident in children with microtia or other combinations of CFM-related facial features.

CONCLUSIONS:

Cognitive and motor scores were similar for preschool-aged children with and without CFM. However, children with CFM scored lower than controls on language measures. We recommend early monitoring of language to identify preschoolers with CFM who could benefit from intervention.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Goldenhar Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Humans / Infant País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Goldenhar Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Humans / Infant País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article