Angelman syndrome

Angelman syndrome (AS) is a genetic condition that causes problems with the way a child's body and brain develop. The syndrome is present from birth (congenital). However, it often isn't diagnosed until about 6 to 12 months of age. This is when development problems are first noticed in most cases.

Causes

This condition involves the gene UBE3A .

Most genes come in pairs. Children one from each parent. In most cases, both genes are active. This means information from both genes is used by the cells. With the UBE3A gene, both parents pass it on, but only the gene passed on from the mother is active.

Angelman syndrome most often occurs because UBE3A passed on from the mother doesn't work the way it should. In some cases, AS is caused when two copies of UBE3A gene come from the father, and none come from the mother. This means neither gene is active, because they both come from the father.

Symptoms

In newborns and infants:

• Loss of muscle tone (floppiness)
• Trouble feeding
• Heartburn (acid reflux)
• Trembling arm and leg movements

In toddlers and older children:

• Unstable or jerky walking
• Little or no speech
• Happy, excitable personality
• Laughing and smiling often
• Light hair, skin, and eye color compared to rest of family
• Small head size compared to body, flattened back of head
• Severe intellectual disability

  Severe intellectual disability

  Intellectual disability is a condition diagnosed before age 18 that includes below-average intellectual function and a lack of skills necessary for d...

   

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• Seizures

  Seizures

  A seizure is the physical findings or changes in behavior that occur after an episode of abnormal electrical activity in the brain. The term "seizure...

   

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• Excessive movement of the hands and limbs
• Sleep problems
• Tongue thrusting, drooling
• Unusual chewing and mouthing movements
• Crossed eyes

  Crossed eyes

  Strabismus is a disorder in which both eyes do not line up in the same direction. Therefore, they do not look at the same object at the same time. ...

   

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• Walking with arms uplifted and hands waving

Most children with this disorder don't show symptoms until about 6 to 12 months. This is when parents may notice a delay in their child's development, such as not crawling or starting to talk.

Children between two and five years of age start to show symptoms such as jerky walking, happy personality, laughing often, no speech, and intellectual problems.

Exams and Tests

Genetic tests may diagnose Angelman syndrome. These tests look for:

• Missing pieces of chromosomes
• DNA test to see if copies of the gene from both parents are in an inactive or active state
• Gene mutation in the mother's copy of the gene

Other tests may include:

• Brain MRI

  Brain MRI

  A magnetic resonance imaging (MRI) scan is an imaging test that uses powerful magnets and radio waves to create pictures of the body. It does not us...

   

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• EEG
  

  EEG

  An electroencephalogram is a test to measure the electrical activity of the brain.

   

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Treatment

There is no cure for Angelman syndrome. Treatment helps to manage health and development problems caused by the condition.

• Anticonvulsant medicines help control seizures
• Behavior therapy helps manage hyperactivity, sleep problems, and development problems
• Occupational and speech therapy manage speech problems and teach living skills
• Physical therapy helps with walking and movement problems
  

Support Groups

Angelman Syndrome Foundation: www.angelman.org

ASSERT: www.angelmanuk.org

Outlook (Prognosis)

People with AS live close to a normal lifespan. Many have friendships and interact socially. Treatment helps improve function. People with AS can't live on their own. However, they may be able to learn certain tasks and live with others in a supervised group home.

Possible Complications

Complications may include:

• Severe seizures
• Gastroesophageal reflux (heartburn)
• Scoliosis (curved spine)
• Accidental injury due to uncontrolled movements

When to Contact a Medical Professional

Call your health care provider if your child has symptoms of this condition.

Prevention

There is no way to prevent Angelman syndrome. If you have a child with AS or a family history of the condition, you may want to talk with your health care provider before becoming pregnant.