The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity

J Med Genet. 2000 Mar;37(3):219. doi: 10.1136/jmg.37.3.219.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Cardiomyopathy, Dilated / diagnosis
  • Cardiomyopathy, Dilated / genetics*
  • Deafness / diagnosis
  • Deafness / genetics*
  • Diagnostic Errors
  • Eye Diseases, Hereditary / diagnosis
  • Eye Diseases, Hereditary / genetics*
  • Female
  • Genetic Heterogeneity*
  • Humans
  • Male
  • Obesity / diagnosis
  • Obesity / genetics*
  • Pedigree
  • Syndrome
  • Vision Disorders / diagnosis
  • Vision Disorders / genetics