Blindness in schoolchildren: importance of heredity, congenital cataract, and prematurity

• Published in: British journal of ophthalmology 1987-08, Vol.71 (8), p.578-584
• Main Authors: Phillips, Calbert I, Levy, Anthony M, Newton, Marjorie, Stokoe, N Leslie
• Format: Article
• Language: English
• Subjects: Adolescent; Biological and medical sciences; Birth Weight; Blindness - etiology; Blindness - genetics; Cataract - congenital; Child; Child, Preschool; Humans; Infant, Newborn; Infant, Premature; Intelligence; Medical sciences; Ophthalmology; Optic Atrophy - complications; Probability; Retinopathy of Prematurity - complications; Vision disorders
• ISSN: 0007-1161; 1468-2079
• DOI: 10.1136/bjo.71.8.578

Of 99 children in the Royal Blind School, Edinburgh (which serves Scotland and part of N E England), 15 had optic atrophy (hydrocephalus 4, intracranial haemorrhage 2, prematurity 2, fetal distress 2, birth asphyxia 2, cerebral atrophy 1, cardiac arrest during hernia operation 1, and leukaemia 1). Fourteen had congenital cataract, 12 congenital retinal aplasia (Leber's congenital amaurosis) and 11 retinopathy of prematurity. There were small numbers in many other diagnostic categories, including three with non-accidental head injury. Mental retardation, spasticity, and nystagmus were frequent other correlates in all diagnostic categories. 'Very probably hereditary' was a conservative attribution in 36, while 'probable' seemed appropriate for 12-that is, almost 48% were hereditary. Only about 11 cases might have been prevented through genetic counselling, which testifies to the frequency of autosomal recessive hereditary disease, although no parents were consanguineous.