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Early-onset non-syndromic cataract

MONDO:0011060

Early-onset non-syndromic cataract is a rare, genetic, non-syndromic developmental defect of the eye, with high clinical and genetic heterogeneity, most frequently characterized by bilateral, symmetrical, non-progressive cataracts which present at birth or in early-childhood. Additional ocular manifestations (e.g. anterior segment dysgenesis, colobomas, nystagmus, microcornea, microphthalmia, myopia) may be associated, however other organs/systems are usually not affected.

Also known as: cataract, age-related nuclear, nuclear sclerosis of the lens

11 clinical trials for this condition and its sub-types.

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Sub-types

Early-onset nuclear cataract (1) Autosomal recessive nonsyndromic congenital nuclear cataract (0) Cataract 10 multiple types (0) Cataract 11 multiple types (0) Cataract 13 with adult I phenotype (0) Cataract 14 multiple types (0) Cataract 15 multiple types (0) Cataract 16 multiple types (0) Cataract 17 multiple types (0) Cataract 19 multiple types (0) Cataract 20 multiple types (0) Cataract 21 multiple types (0) Cataract 22 multiple types (0) Cataract 23 (0) Cataract 24 (0) Cataract 25 (0) Cataract 26 multiple types (0) Cataract 27 (0) Cataract 30 (0) Cataract 31 multiple types (0)

Broader categories

Disease (618) Cataract (235) Hereditary disease (172) Eye disorder (97) Human disease (14) Lens disorder (10) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Disease by body system or component (0)
Trials to join now! 8 Not yet finished but already full! 1 Completed 1 Terminated 1
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