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. 2012 Feb 7;18:362–371.

Table 2. Clinical phenotypes and genotypes of the probands of 15 families with TGFBI-linked corneal dystrophies.

Family Phenotype Mutations Age (proband) at examination (years) VA (proband) at examination
NTUH 1
Numerous granules and some stellate opacities
R124H
26
OD: 0.7; OS: 0.7
NTUH 2
Some granular opacities
R124H
29
OD: 1.0; OS: 0.6 (RD s/p SB)
NTUH 16
Numerous granules and some stellate opacities
R124H
60
OD: 0.05; OS: 0.2 with cataract (OU)
NTUH 22
Numerous granules and some stellate opacities
R124H
30
OD: 1.0; OS: 1.0
NTUH 25
Numerous granules and some stellate opacities
R124H
68
OD: 0.5; OS: 0.5 with cataract (OU)
NTUH 6
Some granules with slim lines
R555W
52
OD: 0.5; OS: 0.6
NTUH 3
Bread crumb opacities
R555W
39
OD: 0.5; OS: 0.6
NTUH 4
Bread crumb opacities
R555W
24
OD: 0.4; OS: 0.3
NTUH 5
Bread crumb opacities
R555W
45
OD: 0.5; OS: 0.5
NTUH 7
Reticular superficial opacities
R555Q
21
OD: 0.6; OS: 0.6
NTUH 8
Reticular superficial opacities
R555Q
57
OD: 0.1; OS: 0.1 with cataract (OU)
NTUH 18
Reticular superficial opacities
R555Q
68
OD: 0.05; OS: 0.05 with cataract (OU)
NTUH 9
Flake-dot opacities with lattice lines
R124C
36
OD: 0.3; OS: 0.4
NTUH 15
Superficially diffuse haze with some fine lines
R124C
32
OD: 0.4; OS: 0.4
NTUH 11 Polymorphic dots with lattice lines A546D 39 OD: 0.4; OS: 0.2

OD: right eye, OS: left eye, OU: both eyes. RD s/p SB: retinal detachment after surgery with scleral buckle.