The craniodigital syndrome of Scott: report of a second family

Am J Med Genet. 1990 Oct;37(2):224-6. doi: 10.1002/ajmg.1320370211.

Abstract

We report on a boy with a characteristic combination of facial anomalies, syndactylies of fingers and toes, and mental retardation. Scott et al. (Journal of Pediatrics 78:658-663, 1971) observed 3 brothers with almost identical manifestations. The mother of these patients had bilateral syndactyly of toes 2 and 3. This led the authors to suggest X-linked inheritance. The mother of our patient also has cutaneous syndactyly between the second and third toes, strengthening the hypothesis of X-linked inheritance.

Publication types

  • Case Reports

MeSH terms

  • Face / abnormalities
  • Fingers / abnormalities
  • Follow-Up Studies
  • Genetic Linkage
  • Humans
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Male
  • Skull / abnormalities*
  • Syndactyly / genetics*
  • Syndrome
  • Toes / abnormalities
  • X Chromosome*