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Joint International Conference on Long-term Experiments ...

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usually incompatible with life or c<strong>on</strong>ducive to grave c<strong>on</strong>genital malformati<strong>on</strong>s and<br />

ulterior infantile mortality.<br />

Transplacental transmissi<strong>on</strong> of mother’s acute infecti<strong>on</strong> has a high incidence up to<br />

50% of cases. Chr<strong>on</strong>ic maternal infecti<strong>on</strong> may generate a lower rate of transplacental<br />

transmissi<strong>on</strong> (up to 25% of cases).<br />

In the transplacental transmissi<strong>on</strong> during acute maternal infecti<strong>on</strong>, it is very<br />

important to de<strong>term</strong>ine the moment of infecti<strong>on</strong> related to the stage of pregnancy:<br />

• In the first trimester the disease seldom occurs (10-25% of cases) but is severe,<br />

leading to sp<strong>on</strong>taneous aborti<strong>on</strong>, stillbirth or newborn with severe forms of disease.<br />

• In the sec<strong>on</strong>d trimester of pregnancy, toxoplasmosis occurs in 30-45% of cases,<br />

with in<strong>term</strong>ediary graveness<br />

• In the third trimester, the disease is more frequent (60-65% of cases), but often<br />

benign, with functi<strong>on</strong>al manifestati<strong>on</strong>s, without macroscopic organic<br />

malformati<strong>on</strong>s. During the life of the newborn, he can manifest disorders of<br />

somatic, psychological, intellectual development or functi<strong>on</strong>al-enzymatic defects<br />

There are no certain data referring to the toxoplasmosis manifestati<strong>on</strong> of the c<strong>on</strong>cepti<strong>on</strong><br />

product according to the stage of pregnancy, in the case of mothers with chr<strong>on</strong>ic<br />

reactivated toxoplasmosis by the aforementi<strong>on</strong>ed immunodeppressive factors.<br />

The risk of fetal affecti<strong>on</strong> is c<strong>on</strong>diti<strong>on</strong>ed by the immune resp<strong>on</strong>se of the mother at<br />

the moment of infecti<strong>on</strong>, the number of parasites transmitted to the fetus, and the age of<br />

the fetus at the moment of mother’s sickening. Hence, the lower the gestati<strong>on</strong>al age, the<br />

graver the fetal affecti<strong>on</strong>, but the risk of transmissi<strong>on</strong> is higher.<br />

In the untreated mother the transplacental transmissi<strong>on</strong> rate is 50%, and in the<br />

treated mother 25%. The period with a high risk of developing c<strong>on</strong>genital toxoplasmosis<br />

is c<strong>on</strong>sidered to be between the 10 th and 24 th weeks of pregnancy, and low risk between<br />

the 26 th and 40 th weeks of pregnancy.<br />

If toxoplasmosis occurs in mother in the first trimester of pregnancy, it mostly<br />

results in the death of the fetus and sp<strong>on</strong>taneous aborti<strong>on</strong>, and if it occurs later, it will<br />

manifest in the infant as symptomatic c<strong>on</strong>genital toxoplasmosis either since birth (1 in<br />

10 cases), or <strong>on</strong>ly after m<strong>on</strong>ths/years (9 in 10 cases).<br />

Fig. No.5 – Chr<strong>on</strong>ic Toxoplasmic Encephalopathy<br />

Clinical forms of disease are:<br />

• Severe forms manifested as grave ne<strong>on</strong>atal infecti<strong>on</strong>s with multivisceral affecti<strong>on</strong><br />

(fever or hypothermia, icterus and hepatosplenomegaly, hydro- and/or<br />

microcephaly, intracerebral calcificati<strong>on</strong>s, micro-ophtalmy, nystagmus, strabismus,<br />

477

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