Acampomelic campomelic dysplasia with SOX9 mutation

Am J Med Genet. 2000 Aug 28;93(5):421-5.

Abstract

Acampomelic campomelic dysplasia is a rare clinical variant of the more commonly encountered campomelic dysplasia (CMD1), characterized by absence of long bone curvature (acampomelia). We present a patient with acampomelic CMD1 with a de novo SOX9 missense mutation and report his clinical course to age one year, thereby contributing to genotype-phenotype correlation in CMD1. 2000.

Publication types

  • Case Reports

MeSH terms

  • High Mobility Group Proteins / genetics*
  • Humans
  • Infant
  • Male
  • Mutation, Missense*
  • Osteochondrodysplasias / diagnostic imaging
  • Osteochondrodysplasias / genetics*
  • Radiography
  • SOX9 Transcription Factor
  • Transcription Factors / genetics*

Substances

  • High Mobility Group Proteins
  • SOX9 Transcription Factor
  • SOX9 protein, human
  • Transcription Factors