21q deletion (Q66475): Difference between revisions
From determinar.ia.br - Determine suas informações
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| description / pt-br | description / pt-br | ||
A monossomia 21 é uma anomalia cromossômica caracterizada pela perda de porções variáveis de um segmento do braço longo do cromossomo 21, o que leva a um risco aumentado de defeitos congênitos, atraso no desenvolvimento e déficit intelectual. | |||
| description / en | description / en | ||
Monosomy 21 is a chromosomal anomaly characterised by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit. | |||
Revision as of 14:17, 14 August 2026
Monosomy 21 is a chromosomal anomaly characterised by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_47014571 |
||
| English | 21q deletion |
Monosomy 21 is a chromosomal anomaly characterised by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit. |
