1979
DOI: 10.1111/j.1651-2227.1979.tb18453.x
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Congenital Toxoplasmosis: Late Appearance of Retinal Lesions After Treatment

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Cited by 7 publications
(4 citation statements)
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“…These patients went through two to three month therapeutic cycles, with follow up exams by ophthalmologists, until it was clear that the lesions were healed. Late ocular lesions in children who have congenital toxoplasmosis is widely documented in the literature, including children adequately treated during the first year of life [9,27,28], confirming the necessity of an intensive follow up for these children.…”
Section: Discussionmentioning
confidence: 82%
See 1 more Smart Citation
“…These patients went through two to three month therapeutic cycles, with follow up exams by ophthalmologists, until it was clear that the lesions were healed. Late ocular lesions in children who have congenital toxoplasmosis is widely documented in the literature, including children adequately treated during the first year of life [9,27,28], confirming the necessity of an intensive follow up for these children.…”
Section: Discussionmentioning
confidence: 82%
“…However, most of these children will develop sequelae during childhood or early adult life [4,5,6,7]. Studies have shown that even in infants with subclinical disease at birth and who have had appropriate therapy in the first year of life, there is risk of later appearance of ocular lesions [8,9,10].…”
mentioning
confidence: 99%
“…It was less in the first 4 years of life (approximately 23%) than after 5 years of age (40% to 50%). Thus localized ocular phenomena frequently develop as a late manifestation [245,359,361,400]. De Roever-Bonnet and colleagues [245] postulated that late development of eye lesions may be caused by second infections rather than by relapses, although supporting data for this hypothesis are lacking.…”
Section: Eye Chorioretinitismentioning
confidence: 99%
“…Some infected children without overt disease as neonates may escape serious consequences of the infection; however, a significant number develop chorioretinitis, strabismus, blindness, hydrocephalus or microcephaly, cerebral calcifications, developmental delay, epilepsy, or deafness months or years later. 6,7 Presentation only in the form haemolytic anaemia and hepatosplenomegaly is uncommon.…”
Section: Case Studymentioning
confidence: 99%