Children with a genetic disorder called 22q11.2 deletion syndrome, who frequently are believed to also have autism, often may be misidentified because the social impairments associated with their developmental delay may mimic ...
Sep 18, 2013
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An international team of scientists, including University of Colorado School of Medicine and Children's Hospital Colorado researchers, has discovered a new disease related to an inability to process Vitamin B12.
Sep 5, 2013
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(Medical Xpress)—Between ages three and 10, children with autism spectrum disorder exhibit distinct brain chemical changes that differ from children with developmental delays and those with typical development, according ...
Aug 2, 2013
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(Medical Xpress)—Researchers from The University of Manchester studying a rare and potentially lethal childhood disease – which is the clinical opposite of diabetes - have made an important discovery.
Jun 12, 2013
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Preschool children who have been neglected or emotionally abused exhibit a range of emotional and behavioral difficulties and adverse mother-child interactions that indicate these children require prompt evaluation and interventions, ...
Jun 10, 2013
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(Medical Xpress)—New research from Cardiff and Bristol universities shows that children whose brains process information more slowly than their peers are at greater risk of psychotic experiences.
Apr 26, 2013
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The three most important factors in real estate are location, location, location, and the same might be said for mutations in the gene MECP2, said researchers at Baylor College of Medicine and the Jan and Dan Duncan Neurological ...
Feb 28, 2013
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Researchers from the University of Alberta are helping children with Down syndrome who stutter find their voice and speak with ease.
Feb 25, 2013
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In a new study in mice, a scientific collaboration centered at Brown University lays out in unprecedented detail a neurological signaling breakdown in Angelman syndrome, a disorder that affects thousands of children each ...
Feb 13, 2013
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Thyroid hormone resistance has been linked to mutations in the IGSF1 gene for the first time—surprising researchers who did not suspect it played a role in the maintenance of normal thyroid function.
Jan 16, 2013
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