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Figure 43 | Orphanet Journal of Rare Diseases

Figure 43

From: Corneal dystrophies

Figure 43

Lattice corneal dystrophy type I variant. The amyloid within the corneal stroma from a patient with a homozygous p. Leu527Arg mutation in the TGFBI gene viewed under ultraviolet light after staining the fluorescent dye Thioflavin T.

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