Some infections during pregnancy cross the placenta and damage the fetal brain directly. Others trigger inflammation that does the harm without ever reaching the baby. Knowing which is which — and how to prevent them — is one of the most actionable parts of CP prevention.
Medically reviewed
Updated April 2026
~ min read
TORCH
The infection panel routinely screened during pregnancy
1 in 200
Newborns with congenital CMV — most common congenital infection
Mostly preventable
With vaccination, hygiene, and prenatal screening
Of all the prenatal factors that contribute to cerebral palsy, infections are arguably the most preventable. Vaccines, food safety, hand hygiene, and routine prenatal screening can prevent or catch most of the maternal infections that put fetal brain development at risk. This page covers which infections matter, how they cause CP, and what prevention looks like in practice. For the broader picture, see our overview of cerebral palsy causes or the umbrella guide on prenatal causes of CP.
The infections that contribute to CP fall into a fairly short list, but their mechanisms vary. Some attack the developing brain directly. Others damage it indirectly through inflammation. Some are vaccine-preventable; others require behavioral precautions. Sorting them out is the first step.
Infection is one of several environmental risk factors for CP, working alongside genetic predisposition, oxygen deprivation, premature birth, and maternal health conditions. Understanding how it fits into the broader picture helps explain why prevention strategies layer multiple approaches.
The exact contribution of maternal infections to CP risk is hard to pin down because infections often combine with other factors. A maternal infection can trigger preterm labor, raising risk through prematurity. It can compromise placental function, raising risk through oxygen deprivation. It can directly damage the fetal brain. The same infection might do any or all of these depending on timing, severity, and the host’s genetic background.
Genetic and environmental influences
Genetic factors affect how vulnerable the developing brain is to infection-related insults. Two children exposed to the same maternal CMV infection may have very different outcomes depending on how their genes regulate inflammation, neuronal development, and tissue repair. This is why some children develop CP after seemingly mild prenatal infections while others come through significant infections unaffected. For the deeper picture of how genetics interacts with environmental factors, see genetic factors in cerebral palsy.
Role of maternal health conditions
The interaction between maternal health and infection risk is bidirectional:
Diabetes and obesity impair immune function, raising infection risk and severity.
Autoimmune conditions and immunosuppressive medications can change how the body responds to common infections.
Smoking reduces ciliary clearance in the airway and impairs systemic immune function.
Chronic kidney disease and other conditions raise the risk of urinary tract infections during pregnancy — themselves linked to preterm labor.
Stress and sleep deprivation modestly affect immune function and can compound other risks.
Good prenatal management of underlying maternal conditions reduces infection risk indirectly — another reason routine prenatal care matters.
Maternal infections during pregnancy
The infections most strongly linked to CP are clinically grouped as TORCH infections — an acronym capturing toxoplasmosis, “other” (a catch-all for syphilis, varicella, parvovirus, Zika, and others), rubella, cytomegalovirus, and herpes simplex. Bacterial infections of the membranes or placenta also matter.
These infections share a common feature: they can either reach the fetus directly or trigger maternal inflammation that does the harm without crossing. Modern prenatal care includes routine screening for several of them and prevention strategies for all.
Common infections affecting pregnancy
The infections most strongly linked to CP, with brief notes on each:
Cytomegalovirus (CMV). The most common congenital infection in the U.S., affecting about 1 in 200 newborns. Most maternal CMV infections cause no symptoms, which is why hand hygiene around young children (the main source) matters even when the mother feels fine.
Rubella (German measles). Once a major cause of congenital disability, now rare in countries with universal vaccination. The MMR vaccine before pregnancy is highly effective.
Toxoplasmosis. A parasitic infection from undercooked meat, contaminated soil, or cat feces. Can be transmitted across the placenta, especially when first acquired during pregnancy.
Herpes simplex virus (HSV). Genital herpes can be transmitted during delivery, sometimes with severe consequences. Cesarean delivery is recommended when active lesions are present.
Varicella (chickenpox). Maternal infection during pregnancy can cause congenital varicella syndrome. Vaccination before pregnancy prevents it.
Zika virus. Linked to microcephaly and severe neurological problems when contracted during pregnancy. Travel precautions and mosquito avoidance are key.
Syphilis. Crosses the placenta and causes congenital syphilis with multiple complications. Routine screening catches it; treatment with penicillin clears it.
Group B Streptococcus (GBS). Vaginal colonization that can be passed during delivery. Routine screening at 36 weeks and intrapartum antibiotics prevent newborn infection.
Chorioamnionitis. Bacterial infection of the membranes, often during prolonged labor. A recognized contributor to neonatal sepsis and CP.
Listeria monocytogenes. Foodborne bacteria from soft cheeses, deli meats, or raw seafood. Can cross the placenta and cause sepsis or meningitis in the fetus.
Impact on fetal brain development
The mechanisms by which these infections damage the developing brain:
Direct viral or parasitic infection of fetal brain tissue (CMV, rubella, toxoplasmosis, Zika)
Inflammatory injury from cytokines crossing the placenta even without fetal infection (chorioamnionitis, severe maternal illness)
Vascular injury as inflammation damages blood vessels in the developing brain
Disruption of neuronal migration during critical windows of fetal brain development
Triggering of preterm labor — with prematurity itself raising CP risk
The same infection in two different pregnancies can produce different outcomes depending on timing (first vs. third trimester), severity, maternal immune response, and fetal genetic background.
What prenatal infection screening covers
Standard U.S. prenatal screening typically tests for:
HIV, syphilis, hepatitis B (early pregnancy)
Rubella immunity (first visit)
Group B Strep (~36 weeks)
Targeted testing for CMV, toxoplasmosis, or Zika when symptoms or exposure
Preventing cerebral palsy through infection prevention
Most maternal infections linked to CP are preventable with established public-health tools: vaccines, screening, food safety, hygiene, and prompt treatment when infections do occur. The interventions are well-known and well-studied; the challenge is consistent implementation.
Prevention works best when it’s layered — combining vaccination before pregnancy, screening during prenatal care, safe behaviors throughout pregnancy, and prompt treatment of any infections that do develop. No single measure prevents everything; the combination prevents most.
Prenatal care strategies
What prenatal care contributes to infection prevention:
Pre-pregnancy or first-trimester immunity testing for rubella, varicella, hepatitis B, and other vaccine-preventable diseases.
Vaccination before pregnancy (MMR, varicella) when not already immune. These are live vaccines that can’t be given during pregnancy.
Vaccinations during pregnancy: influenza (any trimester), Tdap (between 27–36 weeks), and COVID vaccines as recommended.
Routine screening for HIV, syphilis, hepatitis B, and group B strep at standard times.
Targeted screening for CMV, toxoplasmosis, or other infections based on exposure history or symptoms.
Education about food safety, hand hygiene, and travel precautions.
Infection prevention methods
Practical steps with the highest impact:
Hand hygiene around young children. Especially important for CMV prevention, since most maternal CMV infections come from contact with toddlers’ saliva or urine.
Avoid sharing food, utensils, or cups with young children. Same reasoning — CMV is in saliva.
Cook meat thoroughly. Reduces toxoplasmosis and listeria risk.
Avoid unpasteurized dairy and soft cheeses. Listeria again.
Wash fruits and vegetables. Reduces toxoplasmosis from soil contact.
Avoid changing cat litter if possible; if not, wear gloves and wash hands.
Use insect repellent in Zika-endemic areas and avoid travel to active outbreak zones.
Beyond CP, maternal infections can produce a range of developmental, neurological, and sensory effects. Understanding the full picture of long-term outcomes helps families navigate post-birth surveillance and early intervention.
The same infection can produce different outcomes depending on timing and severity. CMV in early pregnancy may produce microcephaly, hearing loss, and CP; CMV later in pregnancy might produce only hearing loss or mild developmental differences. Knowing what to watch for guides post-birth follow-up.
Neurological disorders linked to infections
Beyond CP, congenital infections are linked to:
Microcephaly. Smaller-than-typical head circumference, often with brain underdevelopment. Strongly associated with Zika, CMV, and rubella.
Sensorineural hearing loss. CMV is the most common non-genetic cause of hearing loss in children.
Vision impairment. Chorioretinitis (inflammation in the back of the eye) and cataracts are linked to CMV, rubella, and toxoplasmosis.
Seizures. May appear shortly after birth or develop later.
Intellectual and learning differences. Range from mild to significant, depending on extent and timing of infection.
Autism spectrum disorder. Some research suggests elevated rates after certain congenital infections.
Many of these conditions co-occur with CP, which is why children diagnosed with CP often need broader screening for hearing, vision, and cognitive function. For more on this, see our guide on non-motor symptoms of cerebral palsy.
Long-term effects on child health
The long-term effects of congenital infection extend beyond what’s detectable at birth:
Late-onset hearing loss. CMV-related hearing loss can develop or worsen over the first years of life, even when initial hearing screening was normal.
Progressive vision changes. Some toxoplasmosis-related eye damage progresses through childhood.
Learning differences. Often most apparent in school-age years.
Behavioral and emotional concerns. Sometimes secondary to learning or sensory differences.
Increased medical surveillance needs. Affected children typically need ongoing monitoring of neurology, hearing, vision, and development.
Early identification of congenital infection — ideally in the newborn period — opens the door to interventions that improve long-term outcomes.
The CMV problem
CMV is the most common congenital infection in the U.S. yet remains relatively unknown to the public. Most people who get CMV have no symptoms, but maternal CMV during pregnancy can cause hearing loss, vision problems, and CP in the child. Hand hygiene around young children is one of the most effective — and most underused — preventive measures available. Many states now mandate CMV screening for newborns; ask whether your hospital does.
Were maternal infections missed during your prenatal care?
Failure to screen for, recognize, or treat maternal infections during pregnancy can rise to medical malpractice when it leads to preventable injury. Common errors include missed STD screening, failure to vaccinate when indicated, missed urinary tract infections that progress to preterm labor, and untreated chorioamnionitis. Request a free case review.
Wondering if a maternal infection played a role?
Our nurse advocates can help you read your prenatal records and identify whether any infection-related concerns deserve a closer look. Get a free, confidential evaluation.
Frequently asked questions about maternal infections and CP
The infections most strongly linked to CP are the TORCH group: toxoplasmosis, other (syphilis, varicella, parvovirus, Zika), rubella, cytomegalovirus (CMV), and herpes simplex. Bacterial infections of the placenta or membranes (chorioamnionitis), urinary tract infections, and infections during labor itself can also raise risk — mostly through the inflammation they trigger rather than direct fetal infection.
Two main pathways. First, some infections cross the placenta and infect the fetus directly — CMV, rubella, and toxoplasmosis are classic examples. Second, even infections that don’t cross can trigger maternal inflammation, sending chemical signals to the placenta and fetus that disrupt brain development. Both pathways can produce the kind of brain injury that leads to CP.
Untreated infections raise CP risk, can cause other birth defects, and increase the chance of preterm delivery — itself a major CP risk factor. Most pregnancy-related infections are treatable when caught early. Prenatal infection screening exists specifically to identify infections before they cause harm.
Infections during the first trimester have the biggest impact on brain structure because that’s when major brain regions form. Infections in the second and third trimesters more often affect brain function rather than structure. Infections during labor and delivery (chorioamnionitis) can produce inflammatory injury to a brain that was developing normally.
The most effective preventive measures are vaccination (rubella, varicella, flu, Tdap, COVID), routine prenatal screening for infections like syphilis and HIV, food safety practices to avoid toxoplasmosis and listeria, careful hand hygiene to reduce CMV risk, and prompt evaluation of any concerning symptoms during pregnancy.
Yes — smoking impairs maternal immune function and reduces placental blood flow, both of which can amplify the harm of infections. Smoking during pregnancy is independently associated with elevated CP risk and increases the severity of complications when infections do occur. Stopping smoking is one of the highest-impact prenatal interventions available.