2q32q33 deletion (Q60201): Difference between revisions
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A síndrome de microdeleção 2q32q33 é uma anomalia cromossômica associada a um fenótipo variável envolvendo déficit intelectual moderado a grave, atraso significativo na fala, dificuldades persistentes de alimentação, retardo de crescimento e características dismórficas. | |||
| description / en | description / en | ||
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. | |||
Revision as of 07:42, 14 August 2026
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2015922071 |
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| English | 2q32q33 deletion |
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. |
