Clinical anophthalmos (Q46075): Difference between revisions
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13 August 2026
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Revision as of 14:25, 13 August 2026
This refers to the clinical absence of one or both eyes. Both the globe (human eye) and the ocular tissue are missing from the orbit. The absence of the eye will cause a small bony orbit, a constricted mucosal socket, short eyelids, reduced palpebral fissure and malar prominence. Genetic mutations, chromosomal abnormalities, and prenatal environment can all cause anophthalmia. Anophthalmia is an extremely rare disease and is mostly rooted in genetic abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA10.1 |
||
| English | Clinical anophthalmos |
This refers to the clinical absence of one or both eyes. Both the globe (human eye) and the ocular tissue are missing from the orbit. The absence of the eye will cause a small bony orbit, a constricted mucosal socket, short eyelids, reduced palpebral fissure and malar prominence. Genetic mutations, chromosomal abnormalities, and prenatal environment can all cause anophthalmia. Anophthalmia is an extremely rare disease and is mostly rooted in genetic abnormalities. |
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CID11:LA10.1
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dki-india-LA10.1
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Concluído
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13 August 2026
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