Angelman Syndrome: Symptoms, Causes & Early Detection

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.

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.