What is congenital hydrocephalus? Congenital hydrocephalus is a buildup of excess cerebrospinal fluid (CSF) in the brain at birth. The extra fluid can increase pressure in the baby's brain, causing brain damage and mental and physical problems. Finding the condition early and treating it quickly can help limit any long-term problems. But long-term effects mostly depend on what caused the fluid buildup, how bad it gets, and how the baby responds to treatment.
This condition is rare. About 1 out of 1,000 babies is born with it.1 This means that about 999 babies out of 1,000 are not born with it. When hydrocephalus doesn't occur until later in life, it is called acquired hydrocephalus. This topic focuses on hydrocephalus that is present at birth (congenital).
What causes congenital hydrocephalus? This condition is caused by an imbalance between how much CSF the brain makes and how well the body is able to process it.
Normally, CSF flows through and out of chambers of the brain called ventricles, and then around the brain and spinal cord. The fluid is then absorbed by the thin tissue around the brain and spinal cord. But with hydrocephalus, the fluid can't move where it needs to or is not absorbed as it should be. And in rare cases, the brain makes too much fluid.
Congenital hydrocephalus may happen because of Bleeding in the fetus before birth. Certain infections in the mother, such as toxoplasmosis or syphilis. Other birth defects, like spina bifida. What are the symptoms? The clearest symptom of hydrocephalus is a head that is larger than normal. You and your doctor may notice it at birth or within the first several months after your baby is born. But keep in mind that babies' heads grow a lot during the first year. It is only when the head size grows faster than the normal rate for a baby's height and weight that your doctor may think that there is a problem.
The condition may cause the soft spot (fontanelle) on your baby’s head to feel firm or bulge out. If pressure builds in the brain, your baby may Be irritable. Sleep too much. Vomit. Eat very little. How is congenital hydrocephalus diagnosed? Your doctor may suspect that your baby has congenital hydrocephalus if your baby’s head is larger than normal. Your doctor can check for the problem during a physical exam soon after birth.
Your baby may need imaging tests, such as a CT scan, an MRI, or an ultrasound, that can give a picture of the brain with more detail. A fetal ultrasound can sometimes show the problem before birth while the baby is in the uterus.
How is it treated? Early treatment during the baby’s first 3 or 4 months of life is important to help limit or prevent brain damage. Treatment aims to reduce the amount of CSF in the brain to relieve pressure.
In most cases, the doctor places a flexible tube (shunt) in the brain to drain the fluid. The shunt may stay in the brain forever. But it may have to be fixed or replaced later if there is a problem.
After treatment, watch your child closely to make sure that the fluid is draining. You will need to watch for signs of infection or other problems such as Irritability. Poor appetite. Sleeping too much. Vomiting often. Fever and redness along the shunt tract or valve. A child with congenital hydrocephalus is at risk for development problems and may need physical or speech therapy.
It can be hard to wait and see if symptoms will return. And if your child has special needs, it can be a challenge to take care of him or her. Try to take good care of yourself. And ask your doctor about support groups and organizations that can help you and your child.
Paris Tassin's daughter was born with congenital hydrocephalus. It damaged her hearing other wise she is a healthy 4 year old little girl. To see her you would never know she had a disability as hydrocephalus is often considered an invisible disability because it is not able to be seen. Many of us look perfectly fine like myself we can hide the scars under our hair and unless we have surgery nobody knows.