Tony Evers declaring Feb. 15 to be Angelman Syndrome Day. (Above) Lori, Alyssa and Mark Willner are surrounded by many of those who have helped provide services for Alyssa over the years. Lori and ...

Their 3-year-old daughter, Immy, has Angelman Syndrome. It is a rare neurogenetic disorder that affects about one in 15,000 people and causes developmental delays. At the time, Immy was starting ...

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

Feb. 15 is International Angelman Syndrome Day, and the Synk family aims to raise awareness and honor people with the rare ...

to treat Angelman syndrome (AS). "This program has consistently delivered remarkable animal data, reinforcing its potential as a groundbreaking treatment," said Dr. Donald Kohn, Distinguished ...

While the male baby is in the womb ... However, there are few other obvious signs of XXY syndrome. What is Angelman syndrome? Created with Sketch. Angelman syndrome is caused by an over-expression ...

Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are imprinting disorders caused by genetic or epigenetic aberrations of 15q11.2-q13. Their clinical testing is often multitiered; diagnostic ...

A Chabad couple has taken on the incredible mitzvah of adopting a Jewish baby with Down Syndrome. Please help them with the financial support they need. Full Story A Chabad couple has taken on the ...

Scientists in China have unveiled a new method for breeding baby mice with two male parents ... a range of disorders in humans, including Angelman syndrome. "I admire the work — I think it's ...

What are records? Since 2014, The Marshall Project has been curating some of the best criminal justice reporting from around the web. In these records you will find the most recent and the most ...

Another type of genetic disorder involving imprinting, a neurological condition called Angelman syndrome, has also recently been linked to assisted reproduction. Increasingly, doctors have been ...