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Congenital toxoplasmosis

Congenital toxoplasmosis (CTX) is an embryo-fetopathy characterized by ocular, visceral or intracranial lesions secondary to maternal primo-infection by <i>Toxoplasma gondii</i> (Tg).

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PMID (PMCID)
3556131	FEMALE	Infant, Newborn
	[Congenital toxoplasmosis with delayed immune response in children. Diagnostic problems].
	Brade V, Engelhardt A, Harms D. Dtsch Med Wochenschr. 1987;112(21):837-41.
	Clinical suspicion of congenital toxoplasmosis was at first not confirmed serologically (serum titer in the immunofluorescence test [IFT] of 1:1024 and complement-fixation reaction [CFR] of 1:40 equalling those of the mother; IgM-IFT being negative and the IFT and CFR titers significantly falling within two weeks).