Overview
Fetal parvovirus syndrome, also known as congenital parvovirus B19 infection, is a condition caused by maternal infection with human parvovirus B19 (the virus responsible for erythema infectiosum or 'fifth disease') during pregnancy, with subsequent transplacental transmission to the fetus. Parvovirus B19 has a strong tropism for erythroid progenitor cells, meaning it preferentially infects and destroys red blood cell precursors in the fetal bone marrow. This leads to severe fetal anemia, which can result in high-output cardiac failure, generalized edema (hydrops fetalis), and potentially fetal death. The risk of adverse fetal outcomes is highest when maternal infection occurs during the first and second trimesters of pregnancy. Key clinical features of fetal parvovirus syndrome include non-immune hydrops fetalis (characterized by fluid accumulation in at least two fetal body compartments such as ascites, pleural effusion, pericardial effusion, and skin edema), severe anemia, thrombocytopenia, hepatitis, and myocarditis. Some affected fetuses may also develop reticulocytopenia and aplastic crisis. In surviving neonates, manifestations can include congenital anemia, hepatosplenomegaly, and in rare cases, neurological complications. The overall risk of fetal loss following maternal parvovirus B19 infection is estimated at approximately 2-10%, with the risk being greatest between 9 and 20 weeks of gestation. Diagnosis is typically made through detection of parvovirus B19 DNA by PCR in amniotic fluid or fetal blood, combined with ultrasound findings of hydrops fetalis. The primary treatment for severely affected fetuses is intrauterine blood transfusion (IUT) to correct the profound anemia, which has significantly improved survival rates. Serial ultrasound monitoring, including Doppler assessment of the middle cerebral artery peak systolic velocity to detect fetal anemia, is essential for managing pregnancies complicated by parvovirus B19 infection. There is currently no vaccine available to prevent parvovirus B19 infection, and management is largely supportive. Spontaneous resolution of hydrops can occur in some cases without intervention.
Clinical phenotype terms— hover any for plain English:
Neonatal
Begins at or shortly after birth (first 4 weeks)
Treatments
1 availableAmBisome
Empirical therapy for presumed fungal infection in febrile, neutropenic patients
Clinical Trials
View all trials with filters →No actively recruiting trials found for Fetal parvovirus syndrome at this time.
New trials open frequently. Follow this disease to get notified.
Specialists
View all specialists →No specialists are currently listed for Fetal parvovirus syndrome.
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Financial Resources
1 resourcesTravel Grants
No travel grants are currently matched to Fetal parvovirus syndrome.
Community
No community posts yet. Be the first to share your experience with Fetal parvovirus syndrome.
Start the conversation →Latest news about Fetal parvovirus syndrome
No recent news articles for Fetal parvovirus syndrome.
Follow this condition to be notified when news becomes available.
Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
Rare disease caregiving can be isolating. Connect with counseling and peer support.
Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Common questions about Fetal parvovirus syndrome
What is Fetal parvovirus syndrome?
Fetal parvovirus syndrome, also known as congenital parvovirus B19 infection, is a condition caused by maternal infection with human parvovirus B19 (the virus responsible for erythema infectiosum or 'fifth disease') during pregnancy, with subsequent transplacental transmission to the fetus. Parvovirus B19 has a strong tropism for erythroid progenitor cells, meaning it preferentially infects and destroys red blood cell precursors in the fetal bone marrow. This leads to severe fetal anemia, which can result in high-output cardiac failure, generalized edema (hydrops fetalis), and potentially feta
At what age does Fetal parvovirus syndrome typically begin?
Typical onset of Fetal parvovirus syndrome is neonatal. Age of onset can vary across affected individuals.