A long-term follow up was begun in 1982 on offspring of mothers who ac
quired toxoplasmosis during gestation. The 114 newborns were subdivide
d into 3 groups: (1) 26 born to mothers with certain infection; (2) 51
born to mothers with probable infection, and (3) 37 born to mothers w
ith doubtful infection. There were five infections in the first group
(19.2%), three in the second (5.8%) and none in the third. For purpose
s of data elaboration we considered only the 77 offspring of mothers w
ith certain or probable infection. Of these, 2 infected cases out of 5
2 (3.8%) were born to mothers with infection in the first trimester of
pregnancy, 4 out of 21 (19%) in the second trimester, and two out of
four in the third. There were a total of 8 congenital infections (10.4
%). Specific IgM antibodies were revealed in five out of eight infecte
d children (62.5%). Infection was symptomatic in two children (2.6% of
newborns at risk, 25% of infected cases), both born to mothers with i
nfection in the second trimester. In the other six cases diagnosis was
reached by evaluating trends in antibody levels: the percentage of in
fected newborns was higher in the group of maternal infections untreat
ed (50%) or improperly treated (15.4%), compared to those receiving ad
equate treatment (6.9%). We suggest considering as infected children p
resenting specific IgM antibodies and/or antibody titres which do not
become negative, even when symptoms are absent. Therapy with spiramyci
n should be started in all newborns at risk, while the use of sulphami
des and pyrimethamine is justified only after the presence of infectio
n is confirmed. Conclusion Identification of susceptible women before
or early in pregnancy would permit adoption of preventive measures aim
ed at reducing the frequency of congenital infection which is still hi
gh in our case series.