Pyknodysostose--faelles stamfar til en del af danske patienter: Udredning og molekylaergenetisk diagnostik

Annette Haagerup, Mogens Fjord Christensen, Jens Michael Hertz, Torben A Kruse

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Abstrakt

Eight patients with pycnodysostosis from six Danish families were examined for mutations in the cathepsin K gene. Three different mutations are the cause of pycnodysostosis in the six families--five of whom come from Ringkøbing County and one from Vejle County. One mutation has a high frequency in the families from Ringkoebing County. The five families are related through a common ancestor, who introduced the mutation around the year 1100. The disease is described with respect to aetiology, symptoms, prognosis, diagnosis, and symptomatic treatment. Research in pycnodysostosis may bring important knowledge to the understanding of related diseases, such as osteoporosis.
Bidragets oversatte titelPycnodysostosis--common ancestor of some Danish patients. Examination and diagnosis based on molecular genetics
OriginalsprogDansk
TidsskriftUgeskrift for læger
Vol/bind164
Udgave nummer7
Sider (fra-til)887-890
ISSN0041-5782
StatusUdgivet - 2002

Emneord

  • Cathepsins
  • Chromosomes, Human, Pair 1
  • Denmark
  • Dysostoses
  • Female
  • Humans
  • Male
  • Molecular Diagnostic Techniques
  • Mutation
  • Osteosclerosis
  • Pedigree
  • Prognosis

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