Table 3. Glaucoma phenotype of patient with myocilin G376R mutation.
| Ethnic origin | Type of glaucoma | Carrier number | Maximum IOP (mmHg) | Age at diagnosis (year) | Hereditary pattern | Publication year |
|---|---|---|---|---|---|---|
| Japanese |
POAG |
1 |
ND |
45 |
ND |
1997 |
| Irish |
POAG |
5 |
ND |
ND |
AD |
1998 |
| German |
JOAG |
2 |
36 |
14 & 21 |
AD |
1998 |
| Japanese |
POAG & suspect |
8 |
50 |
36.7 (average age) |
AD |
2000 |
| French-Canadian |
Both |
7 |
>50 (4/7) |
34 (median age) |
AD & Sporadic |
2002 |
| UK (Scottish) |
JOAG |
2 |
43 & 52 |
34 & 21 |
AD |
2002 |
| Indian JOAG |
1 |
50.6 |
32 |
Sporadic |
2003 |
|
| French |
ND |
1 |
ND |
ND |
Sporadic |
2003 |
| Swiss | Both & suspect | 13 | 50 | 28–51 | AD | 2008 |
Abbreviations are as follows: AD, Autosomal Dominant; ND, Not Described.