Tetraploidy (Q46843): Difference between revisions
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Latest 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 |
||
| 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. |
Statements
CID11:LD42.1
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dki-india-LD42.1
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Concluído
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13 August 2026
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