Seminars in Pediatric Neurology
Volume 14, Issue 1 , Pages 26-33, March 2007

Trinucleotide Repeat Disorders

  • Richard E. Lutz, MD

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Richard E. Lutz, MD, University of Nebraska Medical Center, Munroe–Meyer Institute for Genetics and Rehabilitation, 985430 Nebraska Medical Center, Omaha, NE 68198-5430.

University of Nebraska Medical Center, Munroe–Meyer Institute for Genetics and Rehabilitation, Omaha, NE.

DNA trinucleotide repeat expansion diseases represent an interesting group of disorders that include a common cause of mental retardation and autism as well as neurodegenerative and other diseases. Many of these disorders have expression in the pediatric age group. The varied molecular mechanisms of these disorders make them model diseases for the study of mitochondrial dysfunction induced apoptosis, abnormal axonal transport induced apoptosis and disrupted transcription of neighboring genes. Clinical variation in the pathogenesis, severity, onset and inheritance of these disorders make them models for clinical study and research.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 10.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1071-9091(06)00163-X

doi:10.1016/j.spen.2006.11.006

Seminars in Pediatric Neurology
Volume 14, Issue 1 , Pages 26-33, March 2007