Expanded phenotype and ethnicity in Setleis syndrome

Am J Med Genet. 1989 Nov;34(3):354-7. doi: 10.1002/ajmg.1320340311.

Abstract

Setleis syndrome, an autosomal recessive disorder characterized by "coarse" face, temporal cutis aplasia, double upper eyelashes, absent lower eyelashes, chronic conjunctivitis, and prominent thick lips, was reported previously in 8 Puerto Rican children. We report on 3 unrelated children (one mentally retarded) with Setleis syndrome who are not of Puerto Rican descent. Two of our patients had imperforate anus, which has not previously been reported. The evolution of the phenotype over time is illustrated.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / ethnology
  • Abnormalities, Multiple / pathology*
  • Chile
  • China / ethnology
  • Europe / ethnology
  • Eyelashes / abnormalities*
  • Face / abnormalities*
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Phenotype
  • Puerto Rico
  • Skin Abnormalities*
  • Syndrome
  • United States