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Angelman Syndrome (cont.)

What is Angelman Syndrome?

Angelman syndrome is a genetic disorder that causes developmental delay and neurological problems. The physician Harry Angelman first delineated the syndrome in 1965, when he described several children in his practice as having "flat heads, jerky movements, protruding tongues, and bouts of laughter."

What are the characteristics, signs, and symptoms of Angelman syndrome?

  • Infants with Angelman syndrome appear normal at birth, but often have feeding problems in the first months of life and exhibit noticeable developmental delays by 6 to 12 months.
  • Seizures often begin between 2 and 3 years of age.
  • Speech impairment is pronounced, with little to no use of words. Individuals with this syndrome often display hyperactivity, small head size,sleep disorders, and movement and balance disorders that can cause severe functional deficits.

Angelman syndrome results from absence of a functional copy of the UBE3A gene inherited from the mother.

Is there any treatment for Angelman syndrome?

There is no specific therapy for Angelman syndrome. Medical therapy for seizures is usually necessary. Physical and occupational therapies, communication therapy, and behavioral therapies are important in allowing individuals with Angelman syndrome to reach their maximum developmental potential.

Medically Reviewed by a Doctor on 4/1/2014

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Angelman Syndrome - Signs and Symptoms Question: What were the signs and symptoms associated with your child's Angelman syndrome?
Angelman Syndrome - Treatment Question: What kinds of treatment or therapy does your child receive for Angelman syndrome?
Source: MedicineNet.com
http://www.medicinenet.com/angelman_syndrome/article.htm

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