Tetraploidy (Q46843): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença causada por dois conjuntos adicionais de cromossomos, com um total de 92 cromossomos. Essa doença comumente resulta em aborto espontâneo durante o primeiro trimestre. Nascidos vivos de indivíduos com tetraploidia são muito raros. Esses casos são caracterizados por dismorfismo facial, crescimento com grave atraso e atraso no desenvolvimento. A confirmação se dá por meio da observação de dois conjuntos adicionais de cromossomos por cariotipagem. | |||
| description / en | description / en | ||
A disease caused by two additional sets of chromosomes, for a total of 92 chromosomes. This disease commonly results in spontaneous abortion during the first trimester. Live births of tetraploidy individuals are very rare. These cases are characterised by facial dysmorphism, severely delayed growth and developmental delay. Confirmation is through observation of two additional sets of chromosomes by karyotyping. | |||
Revision as of 15:41, 13 August 2026
A disease caused by two additional sets of chromosomes, for a total of 92 chromosomes. This disease commonly results in spontaneous abortion during the first trimester. Live births of tetraploidy individuals are very rare. These cases are characterised by facial dysmorphism, severely delayed growth and developmental delay. Confirmation is through observation of two additional sets of chromosomes by karyotyping.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD42.1 |
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| English | Tetraploidy |
A disease caused by two additional sets of chromosomes, for a total of 92 chromosomes. This disease commonly results in spontaneous abortion during the first trimester. Live births of tetraploidy individuals are very rare. These cases are characterised by facial dysmorphism, severely delayed growth and developmental delay. Confirmation is through observation of two additional sets of chromosomes by karyotyping. |
