Congenital aphakia (Q46081): Difference between revisions
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Afacia primária congênita é uma anomalia do desenvolvimento ocular caracterizada pela ausência do cristalino e pode estar associada a anomalias oculares secundárias variáveis (incluindo aplasia/displasia do segmento anterior do olho, microftalmia e, em alguns casos, ausência de íris, displasia retiniana ou esclerocórnea). | |||
| description / en | description / en | ||
Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea). | |||
Revision as of 14:25, 13 August 2026
Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA12.2 |
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| English | Congenital aphakia |
Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea). |
