Ophthalmoacromelic syndrome (Q94956): Difference between revisions
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Microftalmia com anomalias de membros, também conhecida como síndrome oftalmo-acromélica, é um transtorno do desenvolvimento raro caracterizado por microftalmia ou anoftalmia bilateral, sinostose, sindactilia, oligodactilia e/ou polidactilia. | |||
| description / en | description / en | ||
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly. | |||
Revision as of 10:31, 16 August 2026
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1788103611 |
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| English | Ophthalmoacromelic syndrome |
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly. |
