PTEN Hamartoma tumour syndrome (Q92906): Difference between revisions
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Síndrome do tumor hamartoma PTEN (PHTS) é caracterizada por múltiplos hamartomas que podem afetar várias áreas do corpo. Hamartoma é uma malformação semelhante a um tumor benigno, composta de células maduras e tecido normalmente encontrado na área afetada. A PHTS é causada por mutações no gene PTEN. A PHTS inclui virtualmente todos os casos da síndrome de Cowden (também conhecida como síndrome do hamartoma múltiplo) e uma porcentagem de casos de síndrome de Bannayan-Riley-Ruvalcaba, síndrome de Proteus e síndrome semelhante a Proteus. | |||
| description / en | description / en | ||
The PTEN hamartoma tumour syndrome (PHTS) is characterised by multiple hamartomas that can affect various areas of the body. Hamartoma is a benign tumour-like malformations, composed of mature cells and tissue normally found in the affected area. PHTS is caused by mutations of the PTEN gene. PHTS includes virtually all cases of Cowden syndrome (also known as multiple hamartoma syndrome) and a percentage of cases of Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome and Proteus-like syndrome. | |||
Revision as of 08:01, 16 August 2026
The PTEN hamartoma tumour syndrome (PHTS) is characterised by multiple hamartomas that can affect various areas of the body. Hamartoma is a benign tumour-like malformations, composed of mature cells and tissue normally found in the affected area. PHTS is caused by mutations of the PTEN gene. PHTS includes virtually all cases of Cowden syndrome (also known as multiple hamartoma syndrome) and a percentage of cases of Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome and Proteus-like syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_892873372 |
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| English | PTEN Hamartoma tumour syndrome |
The PTEN hamartoma tumour syndrome (PHTS) is characterised by multiple hamartomas that can affect various areas of the body. Hamartoma is a benign tumour-like malformations, composed of mature cells and tissue normally found in the affected area. PHTS is caused by mutations of the PTEN gene. PHTS includes virtually all cases of Cowden syndrome (also known as multiple hamartoma syndrome) and a percentage of cases of Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome and Proteus-like syndrome. |
