Oliver McFarlane syndrome: a 25-year follow-up

Am J Med Genet. 1989 Oct;34(2):199-201. doi: 10.1002/ajmg.1320340213.

Abstract

We describe findings in a 29-year-old woman with Oliver McFarlane syndrome after 25 years of follow-up, and we review findings in six other reported cases. Pigmentary retinal degeneration, trichomegaly, prenatal onset growth failure, anterior pituitary deficiencies, and peripheral neuropathy characterize the condition.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Adult
  • Chromosome Banding
  • Female
  • Follow-Up Studies
  • Hair Diseases / genetics*
  • Humans
  • Hypopituitarism / genetics*
  • Retinal Degeneration / genetics*
  • Syndrome