Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations.
Khan AO, Aldahmesh MA, Alkuraya FS.
Mol Vis. 2011;17:2570-9. Epub 2011 Oct 4.
PMID:22025892
A Novel PGAP3 Gene Mutation-Related Megalocornea Can Be Misdiagnosed as Primary Congenital Glaucoma.