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Diseases

Genetic and Rare Diseases Information Center (GARD)

Xeroderma pigmentosum, type 9


Other Names for this Disease
  • Xeroderma pigmentosum, complementation group 1
  • XP9
  • Xp, group 1
  • XP1
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News & Events


NCATS Co-Sponsored Conferences

  • Xeroderma Pigmentosum and other Diseases of Human Premature Aging and DNA Repair: Molecules to Patients, Tuesday, September 05, 2006
    Location: National Conference Center, Lansdowne, VA
    Description: This meeting was a follow-up of one held in 2004. The purpose of this workshop was to gather leading scientists and clinicians in this very active area of research. The clinical and mechanistic aspects of Cowden's syndrome (CS) and related DNA repair/transcription defective disorders such as xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) were explored. Our goals were to develop new multidisciplinary collaborations, interactions, and relationships that can lead to a greater understanding of the pathophysiological mechanisms involved in these disorders and to conceive new therapeutic strategies for their treatment.

Other Names for this Disease
  • Xeroderma pigmentosum, complementation group 1
  • XP9
  • Xp, group 1
  • XP1
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.