Axenfeld-Rieger Syndrome and Leukoencephalopathy Caused by a Mutation in FOXC1

Pediatr Neurol. 2017 Jan:66:113-114. doi: 10.1016/j.pediatrneurol.2016.08.020. Epub 2016 Sep 9.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Anterior Eye Segment / abnormalities*
  • Anterior Eye Segment / diagnostic imaging
  • Child
  • Eye Abnormalities / complications
  • Eye Abnormalities / diagnostic imaging*
  • Eye Abnormalities / genetics*
  • Eye Diseases, Hereditary
  • Female
  • Forkhead Transcription Factors / genetics*
  • Humans
  • Leukoencephalopathies / complications
  • Leukoencephalopathies / diagnostic imaging*
  • Leukoencephalopathies / genetics*
  • Mutation / genetics*

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors

Supplementary concepts

  • Axenfeld-Rieger syndrome