Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome

Ann Clin Res. 1969 Dec;1(4):314-24.
No abstract available

MeSH terms

  • Adult
  • Age Factors
  • Amyloidosis / genetics*
  • Blood Protein Electrophoresis
  • Brain Diseases
  • Corneal Dystrophies, Hereditary / genetics*
  • Female
  • Finland
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Peripheral Nervous System Diseases / genetics*
  • Skin Diseases / genetics