Table 3 of Sun, Mol Vis 2011; 17:2197-2206.


Table 3. The clinical information of the patients with congenital cataracts and identified mutations.

ID Gene Mutation Gender Age (yrs) at Inheritance Visual acuity (right;left) Cataract types
        exam onset      
QT237 CRYAA c.292G>A male 10 7 AD 0.2; 0.5 lamellar, punctate
QT237 II:1 CRYAA c.292G>A female N/A N/A AD 0.6; 0.7 lamellar, Y-suture
QT261 CRYAA c.350_352delGCT male 5 at birth AD N/A; 0.2 N/A
QT192 CRYAB c.205 C>T male N/A N/A AD N/A N/A
QT286 CRYBA1 c.215+1G>A male 6 at birth AD 0.3; 0.1 lamellar
QT456 CRYBA1 c.272_274delGAG male 19 at birth AD 0.1; 0.1 nuclear
QT174 CRYBA1 c.272_274delGAG female 49 at birth AD FC; FC nuclear
QT268 CRYGD c.106G>C male 40 at birth AD 0.3; 0.2 nuclear
QT427 CRYGS c.77 A>G female 27 at birth sporadic N/A coppock
QT206 GJA3 c.176 C>T female 26 at birth AD 0.6; 0.5 N/A
QT260 GJA3 c.1143_1165del23 female 17 at birth AD 0.4; 0.2 punctate nuclear