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).

Hepatosplenomegaly

Simultaneous enlargement of the liver and spleen.


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PMID (PMCID)
10771960
 MALE Infant
Cholestatic jaundice due to congenital Toxoplasma gondii infection.
Singh S, Lodha R, Passi GR, Bhan MK.
Indian J Pediatr. 1998;65(1):154-7.
A case of congenital toxoplasmosis manifesting as hepatosplenomegaly and cholestatic jaundice in a 4 month old child is reported.