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<title>Medical Xpress: PHYSorg news tagged with: mental retardation</title>
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<description>Medical Xpress internet news portal provides the latest news on Health and Medicine.</description>

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     <title>First steps of synapse building is captured in live zebra fish embryos</title>
   	 <description>Using spinning disk microscopy on barely day-old zebra fish embryos, University of Oregon scientists have gained a new window on how synapse-building components move to worksites in the central nervous system.</description>
     <link>http://medicalxpress.com/news/2013-04-synapse-captured-zebra-fish-embryos.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Thu, 18 Apr 2013 13:04:29 EST</pubDate>
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     <title>Researchers discover new therapy for fragile X chromosome syndrome</title>
   	 <description>Researchers at the University of the Basque Country (UPV/EHU) and the Achucarro neurosciences centre have discovered a new therapy for the fragile X chromosome syndrome. This new therapy proposes the modulation of the cerebral endocannabinoid system in order to ameliorate the symptoms of the disease. &quot;Clearly, a cure as such is not going to be achieved, as it involves a disease of genetic origin, but the fact that, by manipulating in a certain way at a cerebral level in order to obtain an improvement in the symptoms of the disease is something highly positive&quot;, stated Ms Susana Mato, researcher at the Department of Neurosciences at the UPV/EHU and at the Achucarro centre. This scientific finding has just been published in Nature Medicine.</description>
     <link>http://medicalxpress.com/news/2013-04-therapy-fragile-chromosome-syndrome.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 10 Apr 2013 09:17:02 EST</pubDate>
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     <title>Protecting against aging at the molecular level</title>
   	 <description>Research from Western University and Lawson Health Research Institute sheds new light on a gene called ATRX and its function in the brain and pituitary. Children born with ATRX syndrome have cognitive defects and developmental abnormalities. ATRX mutations have also been linked to brain tumors. Dr. Nathalie Bérubé, PhD, and her colleagues found mice developed without the ATRX gene had problems in in the forebrain, the part of the brain associated with learning and memory, and in the anterior pituitary which has a direct effect on body growth and metabolism. The mice, unexpectedly, also displayed shortened lifespan, cataracts, heart enlargement, reduced bone density, hypoglycemia; in short, many of the symptoms associated with aging. The research is published in the Journal of Clinical Investigation.</description>
     <link>http://medicalxpress.com/news/2013-04-aging-molecular.html</link>
	 <category>Medical research</category>
	 <pubDate>Mon, 08 Apr 2013 12:00:05 EST</pubDate>
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     <title>UK: Public OK with creating babies from three people</title>
   	 <description>Britain's fertility regulator says it has found broad public support for in vitro fertilization techniques that allow babies to be created with DNA from three people for couples at risk of passing on potentially fatal genetic diseases.</description>
     <link>http://medicalxpress.com/news/2013-03-uk-babies-people.html</link>
	 <category>Obstetrics &amp; gynaecology</category>
	 <pubDate>Wed, 20 Mar 2013 11:38:51 EST</pubDate>
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     <title>Fragile X makes brain cells talk too much, research shows</title>
   	 <description>The most common inherited form of mental retardation and autism, fragile X syndrome, turns some brain cells into chatterboxes, scientists at Washington University School of Medicine in St. Louis report.</description>
     <link>http://medicalxpress.com/news/2013-02-fragile-brain-cells.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Wed, 20 Feb 2013 12:36:01 EST</pubDate>
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     <title>When good habits go bad: Neuroscientist seeks roots of obsessive behavior, motion disorders</title>
   	 <description>Learning, memory and habits are encoded in the strength of connections between neurons in the brain, the synapses. These connections aren't meant to be fixed, they're changeable, or plastic.</description>
     <link>http://medicalxpress.com/news/2013-02-good-habits-bad-neuroscientist-roots.html</link>
	 <category>Autism spectrum disorders</category>
	 <pubDate>Sat, 16 Feb 2013 13:03:52 EST</pubDate>
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     <title>Single protein targeted as the root biological cause of several childhood psychiatric disorders</title>
   	 <description>A new research discovery has the potential to revolutionize the biological understanding of some childhood psychiatric disorders. Specifically, scientists have found that when a single protein involved in brain development, called &quot;SRGAP3,&quot; is malformed, it causes problems in the brain functioning of mice that cause symptoms that are similar to some mental health and neurological disorders in children. Because this protein has similar functions in humans, it may represent a &quot;missing link&quot; for several disorders that are part of an illness spectrum. In addition, it offers researchers a new target for the development of treatments that can correct the biological cause rather than treat the symptoms. This discovery was published in November 2012 print issue of The FASEB Journal.</description>
     <link>http://medicalxpress.com/news/2012-10-protein-root-biological-childhood-psychiatric.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 31 Oct 2012 20:40:07 EST</pubDate>
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     <title>Study finds large proportion of intellectual disability is not genetically inherited</title>
   	 <description>New research published Online First in The Lancet suggests that a high proportion of severe intellectual disability results from genetic causes that are not inherited. These findings are good news for parents, indicating a low risk of passing on the disorder to further children.</description>
     <link>http://medicalxpress.com/news/2012-09-large-proportion-intellectual-disability-genetically.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 26 Sep 2012 18:30:01 EST</pubDate>
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     <title>Scientists identify gene linked to facial, skull and cognitive impairment</title>
   	 <description>A gene whose mutation results in malformed faces and skulls as well as mental retardation has been found by scientists.</description>
     <link>http://medicalxpress.com/news/2012-07-scientists-gene-linked-facial-skull.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 05 Jul 2012 12:05:22 EST</pubDate>
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     <title>Researchers discover the cause of an inherited form of epilepsy</title>
   	 <description>Researchers at McGill University have discovered the cause of an inherited form of epilepsy. The disease, known as double-cortex syndrome, primarily affects females and arises from mutations on a gene located on the X chromosome. Drs. Susanne Bechstedt and Gary Brouhard of the Department of Biology have used a highly advanced microscope to discover how these mutations cause a malformation of the human brain. The results of their study are published in the journal Developmental Cell.</description>
     <link>http://medicalxpress.com/news/2012-06-inherited-epilepsy.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 21 Jun 2012 12:50:01 EST</pubDate>
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     <title>Youth with ASD have poor postsecondary outcomes</title>
   	 <description>(HealthDay) -- Youth with autism spectrum disorders (ASDs) are at high risk for not participating in postsecondary education or employment, particularly in the first two years after high school, according to a study published online May 14 in Pediatrics.</description>
     <link>http://medicalxpress.com/news/2012-05-youth-asd-poor-postsecondary-outcomes.html</link>
	 <category>Autism spectrum disorders</category>
	 <pubDate>Mon, 14 May 2012 15:50:01 EST</pubDate>
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     <title>Neuroscientists find that two rare autism-related disorders are caused by opposing malfunctions in the brain</title>
   	 <description>(Medical Xpress) -- Most cases of autism are not caused by a single genetic mutation. However, several disorders with autism-like symptoms, including the rare Fragile X syndrome, can be traced to a specific mutation. Several years ago, MIT neuroscientist Mark Bear discovered that this mutation leads to overproduction of proteins found in brain synapses -- the connections between neurons that allow them to communicate with each other.</description>
     <link>http://medicalxpress.com/news/2011-11-neuroscientists-rare-autism-related-disorders-opposing.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Thu, 24 Nov 2011 06:20:24 EST</pubDate>
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     <title>Researchers uncover steps in synapse building, pruning</title>
   	 <description>Like a gardener who stakes some plants and weeds out others, the brain is constantly building networks of synapses, while pruning out redundant or unneeded synapses. Researchers at The Jackson Laboratory led by Assistant Professor Zhong-wei Zhang, Ph.D., have discovered a factor in synapse-building, also showing that the building and pruning processes occur independent of each other.</description>
     <link>http://medicalxpress.com/news/2011-11-uncover-synapse-pruning.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Wed, 16 Nov 2011 15:56:33 EST</pubDate>
	 <guid isPermaLink="false">news240681383</guid>
	 
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     <title>X-linked mental retardation protein is found to mediate synaptic plasticity in hippocampus</title>
   	 <description>Scientists at Cold Spring Harbor Laboratory (CSHL) have solved part of a puzzle concerning the relationship between changes in the strength of synapses &amp;#150; the tiny gaps across which nerve cells in the brain communicate &amp;#150; and dysfunctions in neural circuits that have been linked with drug addiction, mental retardation and other cognitive disorders.</description>
     <link>http://medicalxpress.com/news/2011-10-x-linked-mental-retardation-protein-synaptic.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Wed, 19 Oct 2011 12:37:09 EST</pubDate>
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     <title>China shuts US plant in lead scare: report</title>
   	 <description> An American-owned battery plant in China will remain shut until the end of the year over fears it has caused lead poisoning in local children, the Shanghai Daily reported on Friday.</description>
     <link>http://medicalxpress.com/news/2011-09-china.html</link>
	 <category>Health</category>
	 <pubDate>Fri, 23 Sep 2011 04:23:23 EST</pubDate>
	 <guid isPermaLink="false">news235970590</guid>
	 
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     <title>Bioethicist challenges Bachmann on vaccine claim</title>
   	 <description>(AP) --  A prominent bioethicist has offered $10,000 to charity if Republican presidential candidate Michele Bachmann can prove her claim that a vaccination caused mental retardation.</description>
     <link>http://medicalxpress.com/news/2011-09-bioethicist-bachmann-vaccine.html</link>
	 <category>Other</category>
	 <pubDate>Fri, 16 Sep 2011 14:10:50 EST</pubDate>
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     <title>Workings of brain protein suggest therapies for inherited intellectual disability, autism</title>
   	 <description>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. As the majority of patients with Fragile X Syndrome also display autism-like symptoms, the findings offer hope for treating both conditions.</description>
     <link>http://medicalxpress.com/news/2011-07-brain-protein-therapies-inherited-intellectual.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 21 Jul 2011 13:01:43 EST</pubDate>
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     <title>Researchers solve membrane protein mystery</title>
   	 <description>A University of Wisconsin-Madison research team has solved a 25-year mystery that may lead to better treatments for people with learning deficits and mental retardation.</description>
     <link>http://medicalxpress.com/news/2011-06-membrane-protein-mystery.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Wed, 08 Jun 2011 12:00:06 EST</pubDate>
	 <guid isPermaLink="false">news226752886</guid>
	 
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     <title>Most common form of inherited intellectual disability may be treatable</title>
   	 <description>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 the topic has concluded. It appears in ACS Chemical Neuroscience.</description>
     <link>http://medicalxpress.com/news/2011-05-common-inherited-intellectual-disability-treatable.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Tue, 17 May 2011 13:07:52 EST</pubDate>
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