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Jan and Dan Duncan Neurological Research Institute at Texas Children’s

  • The Jan and Dan Duncan Neurological Research Institute at Texas Children’s will be the first facility of its kind in the United States that will use a multidisciplinary research approach and will be dedicated to understanding the unique issues of a child's brain structure, development patterns and related diseases. It will be a new model of excellence in the study of pediatric cognitive development.
  • Brain-related diseases and injuries are estimated to exceed more than a half-trillion dollars annually in health care, lost productivity and other economic costs.
  • Brain-related disorders account for the majority of our nation’s long-term care costs. When combined with other psychiatric disorders, they account for more hospitalization and prolonged care than almost all other diseases combined.
  • Combining research and clinical treatments, the Jan and Dan Duncan Neurological Research Institute will directly address neurological issues by focusing on cutting-edge research, education and treatment of the neurological disorders that affect children. It also will address the causes of major adult diseases such as Alzheimer’s and Parkinson’s diseases. 
  • Scheduled for completion in 2010, the Jan and Dan Duncan Neurological Research Institute will consist of research labs and a vivarium within its 14 floors and 370,000 square feet of space.
  • Texas Children’s Department of Pediatrics faculty has been at the forefront of identifying genes that cause neurological disorders, including Fragile X syndrome, Angelman syndrome, Charcot-Marie-Tooth disease, Prader-Willi syndrome, spinocerebellar ataxia, inherited ataxias, and the brain malformation lissencephaly.
 

 

Jan and Dan Duncan Neurological Research Institute at Texas Children's

 

 
  • The Jan and Dan Duncan Neurological Research Institute at Texas Children’s will house some of the finest researchers in the world, including Dr. Huda Zoghbi. Dr. Zoghbi and her research group identified MeCP2, or methyl-CpG binding protein 2, as the causative gene in Rett syndrome – an X-chromosome-linked neurological disorder.

 

 


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