Intragenic FOXC1 deletion in a Vietnamese child with Axenfeld-Rieger syndrome: case report and review of literature

Clin Dysmorphol. 2023 Jul 1;32(3):124-128. doi: 10.1097/MCD.0000000000000458. Epub 2023 May 1.
No abstract available

Publication types

  • Review
  • Case Reports

MeSH terms

  • Anterior Eye Segment
  • Child
  • Eye Abnormalities* / diagnosis
  • Eye Abnormalities* / genetics
  • Eye Diseases, Hereditary* / diagnosis
  • Eye Diseases, Hereditary* / genetics
  • Forkhead Transcription Factors / genetics
  • Humans
  • Southeast Asian People

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors

Supplementary concepts

  • Axenfeld-Rieger syndrome