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DOI 10.1034/j.1600-0420.2000.078005569.x

Медицинская библиотека · Acta ophthalmologica Scandinavica · 2000

Ophthalmological findings in children with congenital toxoplasmosis. Report from a Swedish prospective screening study of congenital toxoplasmosis with two years of follow-up.

Fahnehjelm K T, Malm G, Ygge J, Engman M L, Maly E, Evengård B

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Congenital toxoplasmosis may lead to severe visual impairment or neurological sequelae in the child.

PURPOSE: To study the severity of the primary and late ophthalmological dysfunction during a prospective incidence study of congenital toxoplasmosis in the Stockholm and Skåne counties.

METHODS

Blood collected on phenylketonuria (PKU) cards from 40,978 consecutively born children were investigated for antitoxoplasma antibodies. Children with verified congenital toxoplasmosis were treated for 12 months with antiparasitic therapy and followed ophthalmologically, neurologically and serologically every third month.

RESULTS

Three children had congenital toxoplasmosis. Two of these were asymptomatic at birth and would have escaped early detection without screening. One child had unilateral severe visual impairment and CNS involvement. The incidence of congenital toxoplasmosis was less than 1:10,000.

CONCLUSION

Neonatal screening is of importance to diagnose asymptomatic infected children with congenital toxoplasmosis as treatment has been shown to reduce long-term sequelae. Ophthalmological investigations should start early and continue in co-operation with paediatricians.

Для цитирования: Fahnehjelm K T, Malm G, Ygge J, Engman M L, Maly E, Evengård B. Ophthalmological findings in children with congenital toxoplasmosis. Report from a Swedish prospective screening study of congenital toxoplasmosis with two years of follow-up.. Acta ophthalmologica Scandinavica. 2000. DOI: 10.1034/j.1600-0420.2000.078005569.x.

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