17q21.31 deletion (Q51202): Difference between revisions
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A monossomia 17q21.31 (síndrome de microdeleção 17q21.31) é uma anomalia cromossômica caracterizada por atraso no desenvolvimento, hipotonia infantil, dismorfismo facial e comportamento amigável/amável. | |||
| description / en | description / en | ||
Monosomy 17q21.31 (17q21.31 microdeletion syndrome) is a chromosomal anomaly characterised by developmental delay, childhood hypotonia, facial dysmorphism, and a friendly/amiable behaviour. | |||
Revision as of 22:21, 13 August 2026
Monosomy 17q21.31 (17q21.31 microdeletion syndrome) is a chromosomal anomaly characterised by developmental delay, childhood hypotonia, facial dysmorphism, and a friendly/amiable behaviour.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1225666773 |
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| English | 17q21.31 deletion |
Monosomy 17q21.31 (17q21.31 microdeletion syndrome) is a chromosomal anomaly characterised by developmental delay, childhood hypotonia, facial dysmorphism, and a friendly/amiable behaviour. |
