Rare Disease in Amish Children Sheds Light on Common Neurological Disorders
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Rare Disease in Amish Children Sheds Light on Common Neurological Disorders
Researchers investigating a regulatory protein involved in a rare genetic disease have shown that it may be related to epileptic and autistic symptoms in other more common neurological disorders. A team of researchers demonstrated how mutations in the STRAD-alpha gene can cause a disease called PMSE (polyhydramnios, megalencephaly, and symptomatic epilepsy) syndrome, found in a handful of Amish children.
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Tags: Genetic, Neurology, Epilepsy, Autism Spectrum Disorder, Disease and Condition, Protein, Children's Health, disease
Most Recently Shared on May 11, 2010 at 3:54 pm By:
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Rare disease in Amish children sheds light on common neurological disorders
labspaces.net — “So often the rare informs the common. Penn researchers investigating a regulatory protein involved in a rare genetic disease have shown that it may be related to epileptic and autistic symptoms in other more common neurological disorders.” View full resource at labspaces.net
Most Recently Shared on May 12, 2010 at 12:23 pm By:
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