Familial prostate cancer (Q52935): Difference between revisions
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O câncer de próstata familiar é geralmente definido como o agrupamento de pelo menos 2 parentes de primeiro ou segundo grau com câncer de próstata em uma família. O câncer de próstata hereditário é um subconjunto das formas familiares e geralmente é definido como o agrupamento familiar de pelo menos 3 parentes de primeiro grau com a doença, ou dois parentes diagnosticados com menos de 55 anos de idade. Esses critérios devem ser estendidos aos parentes de segundo grau do lado materno para incluir a transmissão ligada ao X da doença. | |||
| description / en | description / en | ||
Familial prostate cancer is usually defined as the clustering of at least 2 first- or second-degree relatives with prostate cancer within a family. Hereditary prostate cancer is a subset of the familial forms and is usually defined as the familial clustering of at least 3 first-degree relatives with the disease, or two relatives diagnosed below the age of 55 years. These criteria must be extended to second-degree relatives on the maternal side in order to include X-linked transmission of the disease. | |||
Revision as of 00:17, 14 August 2026
Familial prostate cancer is usually defined as the clustering of at least 2 first- or second-degree relatives with prostate cancer within a family. Hereditary prostate cancer is a subset of the familial forms and is usually defined as the familial clustering of at least 3 first-degree relatives with the disease, or two relatives diagnosed below the age of 55 years. These criteria must be extended to second-degree relatives on the maternal side in order to include X-linked transmission of the disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1593240346 |
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| English | Familial prostate cancer |
Familial prostate cancer is usually defined as the clustering of at least 2 first- or second-degree relatives with prostate cancer within a family. Hereditary prostate cancer is a subset of the familial forms and is usually defined as the familial clustering of at least 3 first-degree relatives with the disease, or two relatives diagnosed below the age of 55 years. These criteria must be extended to second-degree relatives on the maternal side in order to include X-linked transmission of the disease. |
