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Early Developmental Trajectories in Infants With Neurofibromatosis 1.
Garg, Shruti; Wan, Ming Wai; Begum-Ali, Jannath; Kolesnik-Taylor, Anna; Green, Jonathan; Johnson, Mark H; Jones, Emily.
Afiliación
  • Garg S; Division of Neuroscience and Experimental Psychology, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
  • Wan MW; Royal Manchester Children's Hospital, Central Manchester University Hospitals NHS Foundation, Manchester, United Kingdom.
  • Begum-Ali J; Division of Psychology and Mental Health, School of Health Sciences, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
  • Kolesnik-Taylor A; Centre for Brain and Cognitive Development and Department of Psychology, Birkbeck, University of London, London, United Kingdom.
  • Green J; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, United Kingdom.
  • Johnson MH; Division of Neuroscience and Experimental Psychology, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
  • Jones E; Royal Manchester Children's Hospital, Central Manchester University Hospitals NHS Foundation, Manchester, United Kingdom.
Front Psychol ; 13: 795951, 2022.
Article en En | MEDLINE | ID: mdl-35936291
ABSTRACT

Objective:

To examine the trajectories of cognitive, motor and behavioural development in infants with NF1 compared to infants without a family history of neurodevelopmental difficulties. Study

design:

Infants with NF1 and low-risk controls were recruited from 5 months of age and followed longitudinally. Data from standardised tests was gathered at 5, 10 and 14 months and developmental trajectories of motor, language, behaviour, sleep, social development and parent-infant interaction were examined. Linear mixed modelling was used to estimate group differences in cognitive and behavioural measures over time.

Results:

No group differences were observed on Mullen Scale of Early Learning, overall adaptive functioning, temperament or behavioural measures. There were no group differences observed on measures of social communication or parent-infant interaction. Over the course of development, the NF1 group slept less and took more time to settle to sleep as compared to the control group. Maternal education was significantly associated with cognitive and behavioural developmental outcomes in both groups.

Conclusion:

Cognitive, social and behavioural impairments are a cause of significant functional morbidity in children with NF1. This report is the first study to investigate the trajectories of cognitive, motor and behavioural development in infancy in NF1. Our results demonstrate that overall cognitive and behavioural developmental trajectories of the NF1 group in the infancy period are similar to controls. Given previous reports of delayed development in the NF1 cohort by 40 months, early clinical interventions strategies to promote sleep hygiene may be beneficial to optimise developmental outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Psychol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Psychol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido
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