Robinow syndrome with parental consanguinity

Eur J Pediatr. 1989 Jun;148(7):652-3. doi: 10.1007/BF00441525.

Abstract

We describe the clinical features of Robinow syndrome in the first child of a consanguineous Turkish couple. This observation supports the view that severe vertebral anomalies are a feature of the autosomal-recessive form of Robinow syndrome.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Consanguinity*
  • Dwarfism / genetics*
  • Face / abnormalities
  • Female
  • Humans
  • Infant, Newborn
  • Syndrome