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Robinow syndrome
  1. M A Patton,
  2. A R Afzal
  1. Department of Medical Genetics, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK
  1. Correspondence to:
 Professor M A Patton, Department of Medical Genetics, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK;
 mpatton{at}sghms.ac.uk

Abstract

In 1969, Robinow and colleagues described a syndrome of mesomelic shortening, hemivertebrae, genital hypoplasia, and “fetal facies”. Over 100 cases have now been reported and we have reviewed the current knowledge of the clinical and genetic features of the syndrome. The gene for the autosomal recessive form was identified as the ROR2 gene on chromosome 9q22. ROR2 is a receptor tyrosine kinase with orthologues in mouse and other species. The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.

  • Robinow syndrome
  • fetal facies
  • ROR2 gene
  • TK, tyrosine kinase
  • RTK, receptor tyrosine kinase
  • Ig, immunoglobulin-like
  • CRD cysteine rich domain
  • KD, kringle domain
  • BMP, bone morphogenic proteins
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