Symptoms of Angelman Syndrome

Symptoms of Angelman Syndrome - What is Angelman Syndrome? Angelman syndrome is a genetic disorder, developmental delay and neurological problems out. The physician Harry Angelman syndrome, the first definition in 1965 when he described several children in his practice as flat heads, jerky movements, protruding tongues, and laughter.

Watch See Pict of Symptoms of Angelman Syndrome

Infants with Angelman syndrome appear normal at birth but often have feeding problems in the first months of life and significant delays in the development of 6 to 12 months. Seizures usually begin 2 to 3 years.

Speech impairment occurs with little or no words. People with this syndrome often show cause hyperactivity, microcephaly, sleep disorders and disorders of movement and balance, severe functional deficits. Angelman syndrome in the absence of a functional copy of the UBE3A gene inherited from the mother.

Seeing a child with Angelman syndrome have doctor most no signs or symptoms of the disease at birth. The first sign is Angelman syndrome often delays in development, such as crawling or the lack of babbling, between 6 and 12 months.

If your child seems to have developmental delays or if your child shows signs or symptoms of Angelman syndrome, make an appointment with your child's doctor.