Get exclusive member benefits & effect social change. Join Today
Aicardi syndrome is a rare genetic disorder that interferes with the formation of the corpus callosum, which is the structure that connects the two sides of the brain. In people with Aicardi syndrome, the corpus callosum is either partially or completely missing. The disorder occurs almost exclusively in newborn girls. Medical researchers don’t believe the disorder is passed from the parents to their child.
The exact cause of Aicardi syndrome isn’t known. However, it’s thought to be caused by a first-time mutation in the child’s genes. Since the disorder primarily affects females, researchers believe the mutation specifically occurs on the X chromosome, which is one of the two sex chromosomes. Females have two X chromosomes. Males typically have one X chromosome and one Y chromosome.
People with Aicardi syndrome often have the following:
Not all people with Aicardi syndrome have these features. However, some people may display additional abnormalities in the brain, eyes, and face. The severity of symptoms varies significantly from one person to another. Some have very severe seizures and may not survive past childhood, while others have milder symptoms and may live well into adulthood.
Aicardi syndrome symptoms usually appear in babies between the ages of 2 and 5 months old. Your child may begin jerking or having infantile spasms, a type of seizure that occurs in infants. These seizures can develop into epilepsy later in life. Your child may also develop yellowish spots on their eyes. Lesions on the retina, which is the light-sensitive layer of tissue at the back of the eye, cause these spots.
Other symptoms of Aicardi syndrome include:
Additional symptoms of Aicardi syndrome include rib and spine abnormalities, such as scoliosis. Children with this disorder may also have unusual facial features, such as a flatter nose, larger ears, or a smaller space between the upper lip and nose. Since Aicardi syndrome can result in poorly developed eyes, children may experience impaired vision or blindness.
Researchers have also found that the brains of children with Aicardi syndrome may have fewer folds and grooves than a normal brain. Fluid-filled cysts may also be present in the brain.
Aicardi syndrome most often appears in females as well as in boys with Klinefelter’s syndrome, a condition in which a male has an extra X chromosome. For these reasons, researchers believe the disorder is caused by a defect on the X chromosome.
People normally have 46 chromosomes in each cell. Two of the 46 chromosomes are sex chromosomes, known as X and Y. They help determine whether someone will develop male or female sex characteristics. Females have two X chromosomes, while males usually have one X chromosome and one Y chromosome.
During the normal development of an embryo, there should only be one active X chromosome in each cell. This means that one of the two X chromosomes in a female embryo must randomly deactivate during cell formation. In the case of Aicardi syndrome, researchers think that the deactivation of the X chromosomes fails to alternate randomly. As a result, one X chromosome is active in more than half of the body’s cell formations. This is called “skewed X-inactivation.”
Researchers have yet to determine the exact gene that causes skewed X-inactivation, so the cause of the disorder is still not known. This lack of information also makes it difficult to determine the risk factors for Aicardi syndrome.
Doctors can usually diagnose Aicardi syndrome based on the symptoms. However, since each child may present different symptoms, additional tests may be needed. Some tests that are used to help doctors make a diagnosis include:
There’s no cure for Aicardi syndrome at this time. However, some symptoms can be managed with treatment. The most common method of treatment involves controlling the seizures and spasms brought on by the disorder. There are also programs available to help both children and their parents cope with the intellectual disabilities and developmental delays that usually accompany Aicardi syndrome. Your child’s doctor will likely refer you to a pediatric neurologist for further evaluation. A pediatric neurologist is a doctor who specializes in treating nervous system disorders in children. They can help your child with long-term management of Aicardi syndrome. Doctors in these other fields may also be may also be consulted based on the symptoms and severity of the syndrome:
Children with Aicardi syndrome tend to have a shorter lifespan, but the outlook greatly depends on the intensity of their symptoms. Nearly all children with the disorder have some type of intellectual disability or developmental delay.
However, other symptoms can vary significantly depending on the person. Some children with Aicardi syndrome can speak in short sentences and walk by themselves. Others may need help walking and performing other daily tasks. In these cases, children will likely need a caretaker for the rest of their lives. Talk to your child’s doctor to learn more about your child’s particular outlook.
Written by: Carmella Wint and Matthew Solan
Medically reviewed on: Feb 29, 2016: University of Illinois-Chicago, College of Medicine
Enter your symptoms in our Symptom Checker to find out possible causes of your symptoms. Go.
Enter any list of prescription drugs and see how they interact with each other and with other substances. Go.
Enter its color and shape information, and this tool helps you identify it. Go.
Find information on drug interactions, side effects, and more. Go.
From companies that meet the high standards of service and quality set by AARP.
Members save 10% on the monthly service charge of qualified AT&T wireless plans.
Members pay $9.50 for Regal ePremiere Tickets purchased online.
Members earn points on select Walgreens-brand health and wellness products.
Join or renew today! Members receive exclusive member benefits & affect social change.