1p21.3 deletion (Q105594): Difference between revisions
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| description / pt-br | description / pt-br | ||
Síndrome da microdeleção 1p21.3 é uma anomalia cromossômica extremamente rara caracterizada por atraso grave de fala e linguagem, deficiência intelectual, transtorno do espectro autista. | |||
| description / en | description / en | ||
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterised by severe speech and language delay, intellectual deficiency, autism spectrum disorder. | |||
Revision as of 11:56, 17 August 2026
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterised by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1367610860 |
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| English | 1p21.3 deletion |
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterised by severe speech and language delay, intellectual deficiency, autism spectrum disorder. |
