Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
A rare genetic retinal disorder characterized by bilateral iris coloboma progressive retinal dystrophy and marked loss of vision with or without congenital cataracts. Iridolenticular adhesions scattered retinal pigmented epithelia mottling and mild hypermetropic astigmatism may be associated.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
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Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome?
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