Chimaera 46, XX, 46, XY (Q46932): Difference between revisions
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Doença causada pela fusão embrionária XX e XY ou dois eventos distintos de perda de um cromossomo sexual de um embrião XXY no início do desenvolvimento. Isso resulta em um subconjunto de células no corpo com um cariótipo XX, enquanto outras células demonstram um cariótipo XY. Esta doença pode se manifestar com desenvolvimento genital anormal. | |||
| description / en | description / en | ||
A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development. | |||
Revision as of 15:50, 13 August 2026
A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD56 |
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| English | Chimaera 46, XX, 46, XY |
A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development. |
