Non-Immune Hydrops Fetalis
Hydrops fetalis is a condition in which too much fluid builds up in parts of the fetus’s body during pregnancy. This extra fluid can collect under the skin, in the chest, around the heart, or in the belly. Hydrops is usually found during a routine pregnancy ultrasound exam.
Hydrops describes the fluid buildup, but not what causes it. There are two main types, based on the cause:
Immune hydrops – caused when the pregnant person’s and fetus’s blood types are not compatible. This type is now rare because doctors routinely check blood types during pregnancy and can give medication to prevent it.
Non-immune hydrops fetalis (NIHF) – caused by other conditions, such as genetic conditions, heart problems, infection, or other fetal anomalies. Today, NIHF is the most common type of hydrops fetalis.
Hydrops fetalis is rare. It happens in about 1 in every 1,700 to 3,000 pregnancies. It is a serious condition, and outcomes depend on the cause. NIHF can increase the risk of preterm birth, stillbirth, and health problems for the baby.
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NIHF can happen for different reasons. In most cases, something is affecting the fetus’s ability to balance fluid properly. Some common causes include:
Genetic disorders that affect how the body develops and controls fluid.
Heart problems that can make it harder for the heart to pump blood normally. Growths or masses that block the flow of fluid through the fetus’s body
Liver problems that lower protein levels in the blood, causing fluid to leak out of blood vessels.
Infections during pregnancy, such as Parvovirus, that can cause fetal anemia, heart problems, or damage to blood vessels or organs.
Severe fetal anemia, which causes stress to the fetal heart over time and leads to fluid buildup.
Problems with the placenta, umbilical cord, or amniotic fluid that disrupt fluid balance. Sometimes NIHF has more than one cause. For example, a heart problem may be related to a genetic condition or an infection.
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NIHF is most often found during an ultrasound exam when extra fluid is seen in two or more areas of the fetus’s body.
Doctors may order more tests to look for the potential cause and guide pregnancy care. These tests may include:
Blood tests for the parents to check blood type, blood count, and infections that could affect the fetus
A detailed ultrasound to check for problems in the fetal heart, placenta, and umbilical cord or other structures
A Doppler ultrasound to check for fetal anemia
A fetal echocardiogram to check for heart problems
Genetic testing, usually by amniocentesis, to look for genetic conditions
Finding the cause of NIHF helps guide care during and after birth. It may also help doctors understand the risk in future pregnancies. Sometimes, even with testing, the exact cause is not found.
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The chance of NIHF happening again in a future pregnancy depends on its cause. Some causes have little or no increased risk of recurrence, while certain genetic conditions may have a higher chance of occurring again. Genetic counseling may help families understand their individual risk.
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Yes, in some pregnancies with NIHF, the pregnant person can develop mirror syndrome, a condition in which the pregnant person develops swelling that “mirrors” the swelling in the fetus. It can happen in up to 1 in 3 pregnancies with NIHF.
Symptoms for the pregnant person may include:
Swelling
High blood pressure
Protein in the urine
Headaches
Fluid in the lungs
Symptoms similar to preeclampsia
Mirror syndrome can cause serious complications for the pregnant person. In some cases, treating the cause of hydrops may improve both the hydrops and the pregnant person’s symptoms. In other cases, delivery may be recommended.
NIHF also increases the risk of polyhydramnios (too much amniotic fluid around the fetus) and preterm birth. NIHF often leads to early delivery. Labor may either start early on its own, or early delivery may be needed because it is safer for the pregnant person or fetus.
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How NIHF is managed depends on:
The cause of NIHF
How far along the pregnancy is
The health of the pregnant patient and the fetus
Care is often managed by a team of specialists, including maternal-fetal medicine subspecialists, neonatologists, and genetic counselors.
There is no single treatment approach that works for every pregnancy. Options may include:
Close monitoring
Some pregnancies may be managed with regular ultrasound exams, blood pressure checks, and lab tests. Monitoring is tailored to each pregnancy. In some cases, NIHF may remain stable or improve before birth without treatment.
Fetal treatment
Depending on the cause of NIHF, options may include:
Medication to treat heart problems in the fetus,
Fetal blood transfusion for anemia
Medications for the pregnant patient
Procedures to drain excess fluid from the fetus
These treatments are not right for every pregnancy and may involve risks. When successful, treatment before birth can improve the chances of fetal survival.
Palliative care or abortion
When NIHF is severe or is caused by a condition that cannot be treated, families may choose palliative care (comfort care) for their newborn after delivery. Abortion may be another option in some areas.
These decisions are very personal. The health care team will help families weigh their options and make the decision that is right for them.
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Vaginal birth may be possible in some pregnancies affected by NIHF. However, cesarean delivery is common in pregnancies complicated by NIHF. The safest way to deliver depends on the health of the pregnant person and fetus, the cause and severity of the hydrops, and whether the baby will need urgent treatment after birth.
A cesarean delivery may be advised if:
The fetus or pregnant person is not doing well during labor
The baby will need urgent treatment right after birth
There are other medical concerns
Delivery should take place at a hospital with a higher-level neonatal intensive care unit (NICU) and a team able to care for the newborn. If a family has chosen palliative or comfort care, delivery can take place wherever those services are available.
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The outlook for NIHF varies widely. It depends on the cause, how early it is found, whether it can be treated, and how the fetus responds to treatment.
About 1 in 5 pregnancies affected by NIHF end in miscarriage or stillbirth. The risk is higher when NIHF is found earlier in pregnancy.
Among babies born alive, about one-half (50%) to two-thirds (66%) survive. Some babies who survive may have long-term health challenges, while others do well.
Outcomes may be better when the cause of NIHF is treatable. These include parvovirus and some abnormal fetal heart rhythms and anomalies. This is especially true when treatment is given before birth and hydrops resolves during pregnancy.
Outcomes may be worse when NIHF is linked to genetic disorders or other causes that cannot be treated during pregnancy.
Quick Facts
Non-immune hydrops fetalis (NIHF) is a condition where a fetus has too much fluid in two or more parts of the body. Although rare, it can be serious.
NIHF can be found during an ultrasound exam when extra fluid is seen in the fetus’s body. Doctors may check for infections, heart or other structural problems, or genetic conditions to find the cause and decide on the best treatment.
NIHF may increase the risk of mirror syndrome, a condition where the pregnant patient also develops swelling and other symptoms. NIHF can also increase the risk of early delivery (preterm birth) and too much amniotic fluid (polyhydramnios).
Treatment depends on the cause, the pregnant patient’s health, and how far along the pregnancy is. In some cases, the fetus can be treated during pregnancy.
A specialist team usually manages these pregnancies. Delivery often takes place in a hospital with a neonatal intensive care unit (NICU) for advanced newborn care.
Glossary
Abortion: Taking medication or having a surgical procedure to end a pregnancy so that it does not result in a live birth.
Anemia: A condition caused by a decreased number of red blood cells.
Amniotic fluid: The fluid surrounding the fetus in the uterus that is essential for the fetus’s growth and development.
Blood transfusion: Giving blood from a donor to another person.
Cesarean delivery: Surgery in which a baby is delivered through a cut (incision) in the mother’s uterus.
Doppler ultrasound: A specialized type of ultrasound exam that measures blood flow through a blood vessel.
Fetal echocardiogram: An ultrasound exam that checks the structure and function of the fetal heart.
Genetic Counselor: A healthcare professional trained to help patients and families understand genetic conditions, test results, and options for care.
Genetic disorder: Any disorder caused by a genetic change, an abnormal number or structure of chromosomes, or a combination of genetic and other factors.
Genetic testing: Testing performed to determine if the fetus has a genetic disorder, such as an amniocentesis.
Hydrops: An abnormal amount of fluid collecting in 2 or more parts of the fetal body where it should not be.
Immune hydrops: A type of hydrops that happens when the pregnant person’s immune system attacks the baby’s red blood cells. This can cause severe anemia in the fetus and lead to hydrops
Maternal-fetal medicine subspecialist: An obstetrician with specialized training in caring for people with high-risk pregnancies.
Mirror syndrome: A rare and serious condition in pregnancy where both the pregnant person and baby have swelling from fluid buildup. The pregnant person’s symptoms “mirror” the baby’s, and both need medical care.
Miscarriage: The loss of a pregnancy before 20 weeks of pregnancy.
Neonatal intensive care unit (NICU): A special unit in the hospital that cares for sick or preterm newborns.
Neonatologist: A doctor specializing in the care of newborns with health problems.
Non-immune hydrops fetalis (NIHF): Hydrops, not resulting from the pregnant person’s immune system attacking baby’s red blood cells as in immune hydrops. It may be caused by infection, genetic conditions, or fetal heart or other structural problems.
Palliative care: Medical care focused on comfort and quality of life when a serious condition cannot be cured. It may include managing symptoms and providing emotional support for the baby and family. It may focus on making meaningful memories with the baby without pursuing invasive or life-prolonging treatments.
Parvovirus: A virus that usually causes mild or no symptoms in a pregnant person. Parvovirus infection during pregnancy can be passed to the developing fetus and may cause severe anemia and hydrops in the fetus.
Placenta: A special organ that develops during pregnancy. It allows the transfer of nutrients, antibodies, and oxygen from the pregnant person to the fetus. It also makes hormones that support the pregnancy.
Preeclampsia: A pregnancy-specific disorder that causes elevated blood pressure and protein in the urine.
Preterm: Before 37 weeks of pregnancy. Preterm contractions are those that occur before 37 weeks, preterm labor is labor (contractions that cause cervical change) that happens before 37 weeks, and preterm birth is birth that occurs before 37 weeks.
Polyhydramnios: A condition during pregnancy where there is too much amniotic fluid (fluid that surrounds the baby) in the womb.
Stillbirth: Death of a fetus before delivery after 20 weeks of pregnancy.
Ultrasound exam: Use of sound waves to create images of internal organs or the fetus during pregnancy.
Umbilical Cord: The structure linking the growing fetus to the placenta; it contains blood vessels that bring oxygen and nutrients to the fetus and remove waste products.
Content Last Updated: September 2026