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In response to a recent increase in media interest in lupus, the Lupus Foundation of America (LFA) is providing a fact sheet about the disease. For additional information, please visit the LFA website at www.lupus.org.
Washington, July 8 : Researchers at Baylor College of Medicine have found a mutation in a single gene to be responsible for catastrophic epilepsy - characterized by severe muscle spasms, persistent seizures, mental retardation and sometimes autism.
Epilepsy poses a burden to India having a huge population of 110 crores. There are 12 million people with epilepsy alive in India. This is similar to a population of Norway or Sweden.
Catastrophic epilepsy – characterized by severe muscle spasms, persistent seizures, mental retardation and sometimes autism – results from a mutation in a single gene, said Baylor College of Medicine (www.bcm.edu) researchers in a report that appears in the current issue of the Journal of Neuroscience.The BCM department of neurology team replicated the defect in mice, developing a mouse model ...
Catastrophic epilepsy - characterized by severe muscle spasms, persistent seizures, mental retardation and sometimes autism - results from a mutation in a single gene, said Baylor College of Medicine researchers in a report that appears in the current issue of the Journal of Neuroscience.
Most headaches among children are benign and disappear as the child gets older, but still warrant a doctor's attention.
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Catastrophic epilepsy -- characterized by severe muscle spasms, persistent seizures, mental retardation and sometimes autism -- results from a mutation in a single gene, researchers report.
Childhood drownings and near-drownings can happen in a matter of seconds and typically occur when a child is left unattended or during a brief lapse in supervision. Two minutes after submersion, a child will lose consciousness. Irreversible brain damage occurs after four to six minutes and determines the immediate and long-term survival of a child.
Melissa Hall went through her struggle with the rare disease chiari malformation alone.
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