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lattice corneal dystrophy type 3A
Genetics:
- autosomal dominant
- associated with defects in TGFBI
Differential diagnosis:
- clinically resembles lattice corneal dystrophy type 3, but differs in that its age of onset is 70-90 years.
General
corneal disease (keratopathy)
genetic disease of the eye
Database Correlations
OMIM 608471
References
OMIM :accession 608471