Inherited Intellectual Disability

Fragile X protein linked to nearly 100 genes involved in autism

Doctors have known for many years that patients with fragile X syndrome, the most common form of inherited intellectual disability, are often also diagnosed with autism. But little has been known about how the two diagnoses ...

Genetics created Dec 12, 2012 | popularity 4 / 5 (4) | comments 0 | with audio podcast

A striking link is found between the Fragile-X gene and mutations that cause autism

A team led by scientists at Cold Spring Harbor Laboratory (CSHL) publishes research today indicating a striking association between genes found disrupted in children with autism and genes that are targets of FMRP, the protein ...

Genetics created Apr 25, 2012 | popularity not rated yet | comments 0 | with audio podcast

Gene mutations in fruit flies help shed light on inherited intellectual disability in humans

Clumsy fruit flies with poor posture are helping an international team of scientists understand inherited intellectual disability in humans – and vice versa.

Genetics created Jul 04, 2011 | popularity 5 / 5 (1) | comments 1 | with audio podcast

Early menopause in mice: A model of human POI

(Medical Xpress)—Scientists have established a genetic mouse model for primary ovarian insufficiency (POI), a human condition in which women experience irregular menstrual cycles and reduced fertility, ...

Genetics created Aug 30, 2012 | popularity not rated yet | comments 0 | with audio podcast

Fragile X syndrome can be reversed in adult mouse brain

A recent study finds that a new compound reverses many of the major symptoms associated with Fragile X syndrome (FXS), the most common form of inherited intellectual disability and a leading cause of autism. The paper, published ...

Neuroscience created Apr 11, 2012 | popularity 5 / 5 (2) | comments 0 | with audio podcast

Study links Fragile X Syndrome proteins and RNA editing mistakes at nerve-muscle junction

The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of autism. Understanding ...

Neuroscience created Oct 30, 2011 | popularity 5 / 5 (1) | comments 0 | with audio podcast

New insight into fragile gene

(Medical Xpress) -- New research could change the way health professionals identify and treat late-onset dementia.

Neuroscience created Jul 22, 2011 | popularity not rated yet | comments 0 | with audio podcast

Workings of brain protein suggest therapies for inherited intellectual disability, autism

Researchers now have a much clearer understanding of how mutations in a single gene can produce the complex cognitive deficits characteristic of Fragile X Syndrome, the most common inherited form of intellectual disability. ...

Medical research created Jul 21, 2011 | popularity 4 / 5 (2) | comments 0 | with audio podcast

Autism research may be about to bear fruit

(AP) -- More than $1 billion has been spent over the past decade researching autism. In some ways, the search for its causes looks like a long-running fishing expedition, with a focus on everything from genetics ...

Autism spectrum disorders created Apr 09, 2012 | popularity not rated yet | comments 0

Most common form of inherited intellectual disability may be treatable

Advancements over the last 10 years in understanding intellectual disability (ID, formerly mental retardation), have led to the once-unimaginable possibility that ID may be treatable, a review of more than 100 studies on ...

Neuroscience created May 17, 2011 | popularity 5 / 5 (4) | comments 0

New clinical trial to examine medication to treat social withdrawal in Fragile X and autism

Children and adults with social withdrawal due to Fragile X syndrome, the most common cause of inherited intellectual disability and the most common known single gene cause of autism, may benefit from an experimental drug ...

Diseases, Conditions, Syndromes created Jul 20, 2011 | popularity not rated yet | comments 0


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