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Table 1 Ophthalmological findings of patients with Galloway-Mowat Syndrome [1,2,3,4,5,6,7,8, 10,11,12,13, 15,16,17]

From: Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings

Clinical feature

Number of affected (total: 76)

%

Optic atrophy

53

70%

Nystagmus

37

49%

Strabismus

12

16%

Hypertelorism

7

8%

Epicanthal folds

7

8%

Ptosis

3

4%

Oculomotor apraxia

3

4%

Microphthalmia

3

4%

Retinopathy

3

4%

Hypoplasia of the iris

1

1.3%

Corneal opacification

1

1.3%