What Are the Symptoms of Angelman Disease?

Angelman syndrome manifests in infancy, and it eventually leads to developmental and neurological problems. The syndrome itself develops as the result of a genetic disorder and problems involving chromosome 15. The symptoms remain easily identifiable.
  1. Identification

    • Some of the more common symptoms of Angelman syndrome in infants involve a lack of normal actions like crawling, walking and babbling. They may also exhibit trembling limbs and an inability to balance.

    Features

    • Other symptoms may be physically exemplified in crossed eyes, the development of a small head and a flat spot on the back of the head.

    Effects

    • Due to an inability to coordinate certain activities (such as sucking and swallowing), some infants with Angelman syndrome may experience difficulty nursing.

    Warning

    • Some sufferers may have inherited the syndrome from a parent. Speak with a doctor if you think your child may be at risk.

    Coping

    • While no cure currently exists for Angelman syndrome, medications and therapy help cope with some symptoms. For instance, anti-seizure medicine can help curb the onslaught of seizures, while physical therapy can help rectify coordination problems.

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