Early-onset non-syndromic cataract

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A rare genetic non-syndromic developmental defect of the eye disorder 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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Early-onset non-syndromic cataract?

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