A multi-university team of researchers found that expressive language sampling (ELS) can be useful in measuring outcomes in clinical trials targeting fragile X syndrome (FXS). According to their study, ELS, a set of procedures ...
Mar 24, 2020
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According to a February 13 report from the World Health Organization, the Wuhan coronavirus has stricken more than 46,000 people and has caused over 1,300 deaths since the first cases in Wuhan, China, in December 2019. Now, ...
Feb 26, 2020
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Over half of our genomes are made of repeating elements within DNA. In rare cases, these repeats can become unstable and grow in size. These repeat "expansions" cause neurodegenerative diseases such as ALS and dementia as ...
Feb 17, 2020
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New research has discovered that Down's syndrome, Fragile X syndrome and Williams syndrome are all linked to sleep disruption in very young children, and that sleep plays a crucial role in the development of these children's ...
Jan 16, 2020
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A research team at the University of California, Riverside, has found exposure to sound—not sound reduction—during early development of mice engineered to have Fragile X Syndrome, or FXS, restores molecular, cellular, ...
Nov 6, 2019
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A new stand-alone test can more precisely diagnose people with a common genetic cause of autism than the current testing regime.
Oct 28, 2019
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Researchers have identified a gene mutation that causes developmental delay, intellectual disability, behavioral abnormalities and musculoskeletal problems in children. The newly diagnosed condition, called NKAP-related syndrome, ...
Oct 3, 2019
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A new drug discovered through a research collaboration between the University at Buffalo and Tetra Therapeutics may protect against memory loss, nerve damage and other symptoms of Alzheimer's disease.
Sep 9, 2019
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It was long believed the FMR1 premutation—an excessive number of trinucleotide repeats in the FMR1 gene—had no direct effect on the people who carry it. Until recently, the only recognized effect on the carriers of the ...
Aug 21, 2019
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The lab of Yongchao Ma, Ph.D., from Stanley Manne Children's Research Institute at Ann & Robert H. Lurie Children's Hospital of Chicago, discovered how the genetic defect in fragile X syndrome—a type of autism—delays ...
Jul 23, 2019
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