Figure 41
From: Corneal dystrophies
Lattice corneal dystrophy type I variant. Thicker than usual deposits of eosinophilic amyloid in corneal stroma of patient with a homozygous p. Leu527Arg mutation in the TGFBI gene. Hematoxylin and eosin stain.
Figure 41 | Orphanet Journal of Rare Diseases