Male with 46,XX karyotype (Q46771): Difference between revisions
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Uma doença que afeta homens, caracterizada pelo hipogonadismo hipergonadotrófico, deficiência de testosterona e infertilidade. Esta condição também pode apresentar hipospadia. Esta doença pode estar associada a crossover anormal dos cromossomos sexuais durante a meiose no pai, resultando no gene SRY estar presente em uma ou ambas as cópias do cromossomo X. | |||
| description / en | description / en | ||
A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome. | |||
Revision as of 15:34, 13 August 2026
A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD52.0 |
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| English | Male with 46,XX karyotype |
A disease affecting males, characterised by hypergonadotropic hypogonadism, testosterone deficiency, and infertility. This condition may also present with hypospadias. This disease may be associated with abnormal crossing over of the sex chromosomes during meiosis in the father, resulting in the SRY gene being present on one or both copies of the X chromosome. |
