Clinical features in the neonate suggesting congenital toxoplasmosis1 4 5 8 20
| Central nervous system disease | Microcephaly Hearing impairment Seizures Hydrocephalus Motor deficits Intracranial calcifications |
| Ophthalmological disease with subsequent visual impairment | Microphthalmia Chorioretinitis (usually bilateral) Retinal scarring Strabismus Nystagmus Cataract |
| Hepatic disease | Hepatosplenomegaly Jaundice |
| Cardiorespiratory disease | Pneumonitis Myocarditis |
| Systemic features | Rash (may be ‘blueberry-muffin’) Fever Bone marrow suppression (thrombocytopenia, anaemia) |