NEUROLOGICAL DISORDERS :: Congenital and Hereditary Disorders
What is hydrocephalus?
Hydrocephalus is a condition in which there is a lack of absorption, blockage of flow, or overproduction of the cerebral spinal fluid (CSF) that is found inside the ventricles (fluid-filled areas) of the brain. This may result in a build up of fluid that can cause the pressure inside of the head to increase and the skull bones to expand to a larger-than-normal appearance.
What causes hydrocephalus?
Hydrocephalus occurs in approximately one out of 500 births. The following are the primary reasons why hydrocephalus occurs:
Hydrocephalus can occur either as a condition present at birth (congenital), or it can be acquired later in life. When hydrocephalus is not related to a known genetic cause, it is thought that many factors, both genetic and environmental, contribute to the condition. In a small percentage of children, a single gene defect on the X chromosome, or another chromosome, is responsible for the condition. In these cases, the chance for recurrence is higher.
Causes of acquired hydrocephalus may include the following:
What are the symptoms of hydrocephalus?
The following are the most common symptoms of hydrocephalus. However, each child may experience symptoms differently. Symptoms of hydrocephalus in younger children may include the following:
In cases where hydrocephalus is not congenital, but is due to a tumor, trauma, infection, or other causes, the symptoms typically seen in older children may include the following:
The symptoms of hydrocephalus may resemble other conditions or medical problems. Always consult your child's physician for a diagnosis.
How is hydrocephalus diagnosed?
Hydrocephalus may be diagnosed before birth by prenatal ultrasound, a diagnostic imaging technique which uses high-frequency sound waves and a computer to create images of blood vessels, tissues, and organs. Ultrasounds are used to view internal organs as they function, and to assess blood flow through various vessels. In many cases, hydrocephalus does not develop until the third trimester of the pregnancy and, therefore, may not be seen on ultrasounds performed earlier in pregnancy.
The diagnosis of congenital hydrocephalus may also be made at birth after diagnostic testing. During the examination, the physician obtains a complete prenatal and birth history of the child. He/she may also ask if there is a family history of any hydrocephalus or other medical problems. The physician will also ask about developmental milestones in older children since hydrocephalus can be associated with other neuromuscular disorders. Developmental delays may require further medical follow-up for underlying problems.
The child's head may appear larger than normal. A measurement of the circumference of the child's head is taken and compared to a scale that can identify normal and abnormal ranges.
Diagnostic tests that may be performed to confirm the diagnosis of hydrocephalus include:
Treatment of hydrocephalus:
Specific treatment for hydrocephalus will be determined by your child's physician based on:
The goal of treatment is to reduce the pressure in the child's head and to properly drain the cerebral spinal fluid (CSF). Occasionally, medications or procedures to draw off the extra CSF may be used.
Surgery may be needed for some cases of hydrocephalus. Surgery usually involves placing a mechanical shunting device into the child's head to help drain the extra CSF from the brain and redirect the extra fluid to another part of the body to be absorbed. A common type of shunt is the ventriculoperitoneal shunt.
The shunt consists of three parts:
The shunt redirects the CSF out of the head through the tubing to a location elsewhere in the body where it can be absorbed. The shunt is usually placed behind the ear and the tubing is threaded from behind the ear, under the skin to the area of the abdomen, heart, or lung. Your child's physician will determine the drainage location based on your child's condition, age, and other factors.
Potential complications from the shunts or surgery can include the following:
Other complications may include fever, nausea or vomiting, irritability, headache, redness and swelling along the area of the tubing, or decreased alertness or complaints of being tired. These complications require prompt medical evaluation. Following surgery, you will receive instructions on how to care for your child at home and information about signs or symptoms requiring medical care.
Hydrocephalus can affect the brain and a child's development. The extent of the problem is dependent on the severity of the hydrocephalus and the presence of brain or other organ system problems.
The key to treating hydrocephalus is early detection, treatment, and prevention of infection. A child with hydrocephalus requires frequent medical evaluations to ensure proper shunt function. The medical team works hard with your family to provide education and guidance as your child grows and develops.
Genetic counseling may be recommended by your child's physician to discuss the risk of recurrence in a future pregnancies, as well as prenatal testing for hydrocephalus.
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It is important to remember the health information found on this website is for reference only not intended to replace the advice and guidance of your healthcare provider. Always seek the advice of your physician with any questions you may have regarding a medical condition. If you think you may have a medical emergency, call your physician or 911 immediately.
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