Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome

Clin Genet. 1997 Oct;52(4):231-4. doi: 10.1111/j.1399-0004.1997.tb02553.x.

Abstract

The association of scalp defect, unusual ears and absence of nipples was described by Finlay & Marks as an autosomal dominant trait. We report a new case in a 23-year-old woman. Renal insufficiency and cataract seem to be frequent and must be investigated.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Ear / abnormalities*
  • Face / abnormalities
  • Female
  • Hair / abnormalities
  • Humans
  • Kidney / abnormalities*
  • Nipples / abnormalities*
  • Scalp / abnormalities*
  • Syndrome
  • Tooth Abnormalities / genetics