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Causes of poor eye contact in infants: a population-based study.
Levinsen, Mette; Børresen, Malene Landbo; Roos, Laura; Grønskov, Karen; Kessel, Line.
Afiliação
  • Levinsen M; Department of Ophthalmology, Rigshospitalet, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark. mettelevinsen@gmail.com.
  • Børresen ML; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Roos L; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
  • Grønskov K; Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
  • Kessel L; Department of Ophthalmology, Rigshospitalet, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
BMC Ophthalmol ; 21(1): 388, 2021 Nov 07.
Article em En | MEDLINE | ID: mdl-34743689
ABSTRACT

BACKGROUND:

Establishing eye contact between infants and parents is important for early parent-child bonding and lack of eye contact may be a sign of severe underlying disease. The aim of the study was to evaluate the causes of poor or lacking eye contact in infants.

METHODS:

Cross-sectional study reviewing all referrals of infants ≤1 year of age from January 1rst, 2016 to December 31rst, 2018. Medical information was retrieved from patient files covering pregnancy, birth, diagnostic work-up and ocular parameters such as refraction, visual acuity and structural findings.

RESULTS:

We identified 99 infants with poor or lacking eye contact. The relative frequency of causes was neurologic disease 36.4% (36/99), delayed visual maturation 24.2% (24/99), ocular disease 21.2% (21/99) and idiopathic infantile nystagmus 4.0% (4/99). Fourteen infants had a visual function within age-related norms at first examination despite poor eye contact at the time of referral. Of the infants with available data, 18/27 (33.3%) with neurologic cause, 15/23 (65.2%) with delayed visual maturation and 9/21 (42.9%) with ocular cause had visual acuity within the age-related norm at latest follow-up (0-41 months). In 23 infants, a genetic cause was found.

CONCLUSION:

Poor eye contact in infants may be a sign of severe underlying disease, such as neurological or ocular disease. Close collaboration between pediatric ophthalmologists and neuro-pediatricians are warranted in the management of these infants.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nistagmo Congênito / Doenças Genéticas Ligadas ao Cromossomo X Tipo de estudo: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nistagmo Congênito / Doenças Genéticas Ligadas ao Cromossomo X Tipo de estudo: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2021 Tipo de documento: Article