Jacobsen syndrome is a rare congenital condition that’s caused by the deletion of several genes in chromosome 11. It’s sometimes called partial monosomy 11q. It occurs in about 1 in 100,000 ...

Jacobsen syndrome affects approximately 1 in 100,000 people, according to the National Institutes of Health. It occurs in a person when there is a deletion at the end of one arm of the 11th ...

Jacobsen syndrome affects approximately 1 in 100,000 people, according to the National Institutes of Health. It occurs in a person when there is a deletion at the end of one arm of the 11 th ...

Based on this, researchers tested clonazepam, an anti-anxiety drug, to see whether it treated autism-like symptoms in the Jacobsen syndrome mice by boosting GABAAR.

About half of children born with Jacobsen syndrome, a rare inherited disease, experience social and behavioral issues consistent with autism spectrum disorders. Researchers have developed a mouse ...

Called both Jacobsen Syndrome, after the Danish physician who discovered its cause in 1973, and "11q deletion," it results when a child is born with parts of the 11th chromosome missing.

Researchers at San Diego State and UC San Diego said that they've discovered a link between autism and a rare condition known as Jacobsen Syndrome.

Jacobsen syndrome, also called the 11q terminal deletion disorder, is a contiguous gene disorder caused by the deletion of the end of the long arm of chromosome 11. Intellectual skills range from ...

"It scared me, especially as a new mom -- and that's a new mom of twins. I didn't know what to expect for Laila," Bailey said. "What they were able to tell me, because it was such a rare syndrome ...