Clinical anophthalmos (Q46075): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (7 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
Refere-se a ausência clínica de um ou ambos os olhos. Tanto o globo ocular (olho humano) quanto o tecido ocular estão ausentes na órbita. A falta do olho causará órbita pequena, cavidade mucosa constrita, pálpebras curtas, fenda palpebral reduzida e proeminência malar. Mutações genéticas, anormalidades cromossômicas e o ambiente pré-natal podem todos causar anoftalmia. Anoftalmia é uma doença extremamente rara e é majoritariamente originada por anormalidades genéticas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/614784200 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:LA10.1 | |||||||||||||||
| Property / CURIE: CID11:LA10.1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-LA10.1 | |||||||||||||||
| Property / Canary Token: dki-india-LA10.1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Linked ICD 10 | |||||||||||||||
| Property / Linked ICD 10: Q11.1 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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. |
Statements
CID11:LA10.1
0 references
dki-india-LA10.1
0 references
Concluído
0 references
13 August 2026
0 references
