Toward postnatal reversal of ocular congenital malformations.
Level V
Where this comes from
- Record sourced from PubMed, PMID 24355915.
- Also identified by DOI 10.1172/JCI73560 and PMC identifier 3871257.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Aniridia is a panocular disorder that severely affects vision in early life. Most cases are caused by dominantly inherited mutations or deletions of the PAX6 gene, which encodes a transcription factor that is essential for the development of the eye and the central nervous system. In this issue of the JCI, Gregory-Evans and colleagues demonstrate that early postnatal topical administration of an ataluren-based formulation reverses congenital malformations in the postnatal mouse eye, providing evidence that manipulation of PAX6 after birth may lead to corrective tissue remodeling. These findings offer hope that ataluren administration could be a therapeutic paradigm applicable to some major congenital eye defects.
Medical subject headings
- Aniridia
- Eye Proteins
- Gentamicins
- Homeodomain Proteins
- Oxadiazoles
- Paired Box Transcription Factors
- Repressor Proteins