Early-onset non-syndromic cataract
MONDO:0011060Early-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.
Follow this condition — get notified about new trialsSub-types
Early-onset nuclear cataract
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Autosomal recessive nonsyndromic congenital nuclear cataract
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Cataract 10 multiple types
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Cataract 11 multiple types
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Cataract 13 with adult I phenotype
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Cataract 14 multiple types
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Cataract 15 multiple types
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Cataract 16 multiple types
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Cataract 17 multiple types
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Cataract 19 multiple types
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Cataract 20 multiple types
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Cataract 21 multiple types
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Cataract 22 multiple types
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Cataract 23
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Cataract 24
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Cataract 25
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Cataract 26 multiple types
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Cataract 27
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Cataract 30
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Cataract 31 multiple types
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