8p23.1 deletion (Q104602): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A deleção de 8p23.1 envolve uma deleção parcial do braço curto do cromossomo 8 caracterizada por baixo peso ao nascer, deficiência de crescimento pós-natal, déficit intelectual leve, hiperatividade, anormalidades craniofaciais e defeitos cardíacos congênitos. | |||
| description / en | description / en | ||
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects. | |||
Revision as of 10:27, 17 August 2026
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_933685931 |
||
| English | 8p23.1 deletion |
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects. |
