Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy

Clin Genet. 1973;4(3):173-185. doi: 10.1111/j.1399-0004.1973.tb01140.x.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Aged
  • Amyloidosis / diagnosis
  • Amyloidosis / epidemiology
  • Amyloidosis / genetics*
  • Amyloidosis / mortality
  • Consanguinity
  • Corneal Dystrophies, Hereditary / genetics*
  • Facial Paralysis / genetics*
  • Female
  • Finland
  • Heterozygote
  • Homozygote
  • Humans
  • Kidney Diseases / genetics
  • Male
  • Middle Aged
  • Pedigree
  • Prognosis
  • Sex Factors
  • Skin Manifestations
  • Syndrome