This is a five-month-old baby girl diagnosed with Angelman Syndrome. Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing ...

In some cases, doctors can identify Angelman syndrome before your baby is born through a prenatal ultrasound, by looking at the signs of fetal growth issues. However, current studies have shown ...

Angelman syndrome, which affects 1 in 15,000 people ... severe developmental delays and is typically first noticed when a ...

Four-year-old Tyler Rossow may be a politician in the making. The diminutive Carver redhead has a smile and a wave for everyone he meets. And for those lucky enough to cross ...

Angelman Syndrome is a very rare neurogenetic disorder that occurs in approximately one in 15,000 births, caused by the loss of function of a gene ...

Angelman syndrome is caused by a large deletion of the region of the maternal chromosome that contains UBE3A, or by a DNA sequence change (mutation) in the UBE3A gene inherited from the mother.

We each get two copies of every gene - one copy from each of our parents. But what happens when one of these genes has been "turned off", or imprinted, and the remaining gene is defective?

Considering taking supplements to treat angelman syndrome? Below is a list of common natural remedies used to treat or reduce the symptoms of angelman syndrome. Follow the links to read common ...