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Genetic and Rare Diseases Information Center (GARD)

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Neuronal intranuclear inclusion disease


Other Names for this Disease

  • Neuronal intranuclear hyaline inclusion disease
  • NIID
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Overview

Neuronal intranuclear inclusion disease (NIID) refers to a group of rare degenerative nerve diseases. Signs and symptoms of NIID are widespread, progressive, and usually begin in childhood. NIID causes worsening of many of the body's activities, including balance, movement, talking, eating, and cognition. Currently the cause of NIID is not known. Both sporadic and familial cases have been described.[1][2]

Last updated: 8/17/2011

References

  1. Josephs KA. Neuronal intranuclear inclusion disease. Neurology. 2011 Apr 19;76(16):1368-9; http://www.ncbi.nlm.nih.gov/pubmed/21411743. Accessed 8/17/2011.
  2. McFadden K, Hamilton RL, Insalaco SJ, Lavine L, Al-Mateen M, Wang G, Wiley CA. Neuronal intranuclear inclusion disease without polyglutamine inclusions in a child. J Neuropathol Exp Neurol. 2005 Jun;64(6):545-52; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402362/?tool=pubmed. Accessed 8/17/2011.
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  • The Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.
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Selected Full-Text Journal Articles

Other Names for this Disease
  • Neuronal intranuclear hyaline inclusion disease
  • NIID
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.