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Book of Medical Disorders in Pregnancy - Tintash

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identify<strong>in</strong>g a primary <strong>in</strong>fection<br />

accurately.<br />

Immunity: Infection with CMV confers<br />

immunity <strong>in</strong> the host because persistence<br />

<strong>of</strong> the agent <strong>in</strong> a latent phase and<br />

reactivation <strong>in</strong> response to various<br />

stimuli occurs. Although unusual, a<br />

woman may bear a second child with<br />

congenital <strong>in</strong>fection <strong>of</strong> the same serotype.<br />

S<strong>in</strong>ce cytomegalovirus exists <strong>in</strong><br />

multiple serotypes, re<strong>in</strong>fection <strong>of</strong> a<br />

woman <strong>in</strong> the childbear<strong>in</strong>g age with a<br />

different type can result, <strong>in</strong> the birth <strong>of</strong><br />

another <strong>in</strong>fected <strong>in</strong>fant to the same<br />

mother. These occurrences nevertheless<br />

are very rare. In general after the birth <strong>of</strong><br />

a congenitally <strong>in</strong>fected <strong>in</strong>fant the fetus <strong>in</strong><br />

the subsequent pregnancy is not at<br />

significantly greater risk.<br />

Fetal <strong>in</strong>fection: Intrauter<strong>in</strong>e <strong>in</strong>fection<br />

with CMV is probably the most common<br />

viral <strong>in</strong>fection <strong>of</strong> the human fetus. It has<br />

been estimated that the prevalence <strong>of</strong><br />

CMV <strong>in</strong>fection at birth shows a<br />

frequency <strong>of</strong> 4 to 10 <strong>in</strong>fected <strong>in</strong>fants per<br />

1,000 births. Many po<strong>in</strong>ts <strong>of</strong> similarity<br />

can be found between congenital CMV<br />

and Rubella, but <strong>in</strong> general there is a<br />

lower frequency <strong>of</strong> congenital disease <strong>in</strong><br />

CMV with a preponderance <strong>of</strong> damage<br />

to the CNS <strong>in</strong> contrast to the<br />

comb<strong>in</strong>ation <strong>of</strong> malfor-mation and<br />

congenital disease which is to be found<br />

<strong>in</strong> <strong>in</strong>fants with congenital Rubella.<br />

Another common feature is that the<br />

<strong>in</strong>fant may be excret<strong>in</strong>g virus at birth yet<br />

show no symptoms. The majority rema<strong>in</strong><br />

unaffected as they grow older.<br />

Approximately one <strong>in</strong> 10 <strong>of</strong> congenitally<br />

<strong>in</strong>fected <strong>in</strong>fant develops symptoms. The<br />

fulm<strong>in</strong>at<strong>in</strong>g illness may present with<br />

hepatosplenomegaly, jaundice, petechial<br />

rash and low birthweight. The <strong>in</strong>fant<br />

may also be premature. The mortality<br />

168<br />

rate is high, particularly if CNS<br />

<strong>in</strong>volvement is prom<strong>in</strong>ent or respiratory<br />

distress is present. The prognosis for<br />

<strong>in</strong>fants with jaundice and thrombocytopenic<br />

purpura alone is better than for<br />

those who have CNS <strong>in</strong>volvement. In<br />

many <strong>in</strong>fants with the former symptoms<br />

recovery is complete <strong>in</strong> 6 to 8 weeks, but<br />

there is always the possibility that other<br />

symptoms may develop later. The<br />

neurological symptoms are <strong>of</strong> the<br />

greatest consequence both <strong>in</strong> the short<br />

terms and long terms. Microcephaly may<br />

be obvious at birth or become apparent<br />

later <strong>in</strong> <strong>in</strong>fancy. Cerebral diplegia,<br />

spasticity and fits present<strong>in</strong>g early <strong>in</strong> life<br />

usually have a bad prognosis. Henshaw<br />

et al (1973) found a higher <strong>in</strong>cidence <strong>of</strong><br />

CMV <strong>in</strong>fection determ<strong>in</strong>ed by the presence<br />

<strong>of</strong> CF antibody <strong>in</strong> children with<br />

undiagnosed seizures and microcephaly<br />

than <strong>in</strong> patients with genetically determ<strong>in</strong>ed<br />

CNS disease and <strong>in</strong> a control<br />

group <strong>of</strong> normal children.<br />

Fig13.3: shows CMV <strong>in</strong>fection rash on<br />

the body<br />

Toxoplasmosis: Toxoplasma gondii is a<br />

parasite which has a proliferative<br />

(<strong>in</strong>vasive) phase and a cystic (resistant)<br />

phase. The resistant phase is formed <strong>in</strong><br />

response to the immune reaction <strong>of</strong> the<br />

host. The mode <strong>of</strong> <strong>in</strong>fection is unknown.<br />

The <strong>in</strong>fection occurs <strong>in</strong> most parts <strong>of</strong> the<br />

world but is particularly prevalent <strong>in</strong><br />

warm and humid climates.

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