2007
DOI: 10.1016/j.jaapos.2007.01.107
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Babies Count: The national registry for children with visual impairments, birth to 3 years

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Cited by 86 publications
(75 citation statements)
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“…Series of T2W and flair coronal magnetic resonance images from 4 children who all manifested typical features of dorsal stream dysfunction, showing evidence posterior periventricular white matter disease in very similar distributions [26]. [28][29][30] and may even be under-estimated in prevalence studies. A study in Northern Ireland [28] identified visually impaired children from a number of sources including hospital and community pediatric records as well as statutory records.…”
Section: A Epidemiology Of Cerebral Visual Impairment In Childrenmentioning
confidence: 99%
See 1 more Smart Citation
“…Series of T2W and flair coronal magnetic resonance images from 4 children who all manifested typical features of dorsal stream dysfunction, showing evidence posterior periventricular white matter disease in very similar distributions [26]. [28][29][30] and may even be under-estimated in prevalence studies. A study in Northern Ireland [28] identified visually impaired children from a number of sources including hospital and community pediatric records as well as statutory records.…”
Section: A Epidemiology Of Cerebral Visual Impairment In Childrenmentioning
confidence: 99%
“…Only 22% were registered as being visually impaired, indicating that prevalence data based on statutory records often underrepresent visual impairment due to damage to the brain. This may be improving in the USA where a recent report based on the national 'Babies Count' register of visually impaired children aged 0-3 years found CVI to be the commonest form of visual impairment [30].…”
Section: A Epidemiology Of Cerebral Visual Impairment In Childrenmentioning
confidence: 99%
“…1,2,3 Children with bilateral ON hypoplasia usually present in infancy with poor vision and nystagmus, while unilateral or asymmetric ON hypoplasia may be detected later due to strabismus. 4,5 Indirect ophthalmoscopy is usually sufficient to diagnose severe ON hypoplasia, but in mild to moderate cases, diagnosis is more challenging.…”
Section: Introductionmentioning
confidence: 99%
“…Γενικά, ο αλμπινισμός εμφανίζεται σε συχνότητα 1:17.000, ανεξαρτήτως φύλου και εθνοτικής προέλευσης, ενώ περίπου 1 στα 70 άτομα φέρουν ένα γονίδιο του ΟΔΑ (Hatton, Schwietz, Boyer, & Rychwalski, 2007). Κατ' εξαίρεση, ο φυλοσύνδετος ΟΑ διαγιγνώσκεται μόνο στους άρρενες, συναρτήσει της μεταβολής του χρωμοσώματος Xp22.3.…”
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