Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations

Eur J Hum Genet. 2009 Dec;17(12):1527-39. doi: 10.1038/ejhg.2009.93. Epub 2009 Jun 10.

Abstract

Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant disorder, which encompasses a range of congential malformations affecting the anterior segment of the eye. ARS shows genetic heterogeneity and mutations of the two genes, PITX2 and FOXC1, are known to be associated with the pathogenesis. There are several excellent reviews dealing with the complexity of the phenotype and genotype of ARS. In this study, we will attempt to give a brief review of the clinical features and the relevant diagnostic approaches, together with a detailed review of published PITX2 and FOXC1 mutations.

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / therapy
  • Animals
  • Anterior Eye Segment / abnormalities
  • Anterior Eye Segment / embryology
  • Forkhead Transcription Factors / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Mutation / genetics*
  • Syndrome
  • Transcription Factors / genetics*

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors
  • Homeodomain Proteins
  • Transcription Factors
  • homeobox protein PITX2