PTEN Hamartoma tumour syndrome (Q92906): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_892873372
0 references
dki-india-ID_892873372
0 references
Concluído
0 references
