A family with radio-ulnar synostosis, scoliosis, and thick vermilion of lips: a novel syndrome or variant of Giuffrè-Tsukahara syndrome?

Am J Med Genet A. 2012 Aug;158A(8):2036-42. doi: 10.1002/ajmg.a.35478. Epub 2012 Jul 11.

Abstract

We report on a three-generation Chinese family presenting with a recognizable condition consisting of radio-ulnar synostosis, short stature, scoliosis, distinctive craniofacial features (thick vermilion to the lips, prominent eyes, and flat malar region), and a shortened and thickened femur neck. The inheritance of the trait was presumably autosomal dominant. The lack of microcephaly in the family suggested a variant of Giuffè-Tsukahara syndrome but could represent variability

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Adult
  • Aged
  • Child
  • Female
  • Humans
  • Lip Diseases / genetics*
  • Male
  • Scoliosis / genetics*
  • Syndrome
  • Synostosis / genetics*