Table 2.

Ocular anomalies and systemic diagnosis of the affected patients (20/63) with cataract are listed.

Ocular anomalies and systemic diagnosis		N
Complex ocular anomalies	Complex anterior segment dysgenesis (microcornea, posterior embryotoxon, posterior synechiae)	1
	PAX6 mutation∗ (aniridia, persistent tunica vasculosa lentis, macular hypoplasia)	1
Extraocular anomalies	Heart defects (microcornea n = 1∗)	4
Extraocular diseases	Juvenile rheumatic arthritis with chronic uveitis	1
	Nonclassified muscular dystrophy	1
Syndromes	Sakoda complex (agenesis of the corpus callosum and encephalocele, cleft palate, hypoplasia of the right optic nerve)	1
	Down syndrome (vitreous opacities n = 1)	2
	Dysmorphic syndromes of unknown origin (microcornea n = 1)	3
	Marden-Walker syndrome	1
	Lowe syndrome∗ (persistent tunica vasculosa lentis)	1
	Oculo-facio-cardio-dental syndrome	1
Varia	Prematurity of the newborn Gestational age: 31 weeks n = 2, 36 weeks n = 1 (laser scars due to the treatment of retinopathy of prematurity)	3

N: patient number. ^∗Diagnosis of aphakic glaucoma during follow-up period.