19p13.12 deletion (Q65356): 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 síndrome de microdeleção 19p13.12 é uma anomalia cromossômica associada a atraso de desenvolvimento moderado a grave, atraso de linguagem, perda auditiva neurossensorial e/ou condutiva bilateral e dismorfismo facial. | |||
| description / en | description / en | ||
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism. | |||
Revision as of 13:04, 14 August 2026
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1258292853 |
||
| English | 19p13.12 deletion |
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism. |
