Peutz-Jeghers syndrome
Term · Oncology and biomedicine · MLC-T-ONC-006562
A rare genetic disorder in which many polyps (abnormal growths of tissue) form in the lining of the gastrointestinal tract, and dark-colored spots appear on certain areas of the skin, such as around the mouth, eyes, and nose. People with Peutz-Jeghers syndrome have a very high risk of developing gastrointestinal cancer and other types of cancer, including cancers of the breast, pancreas, ovary, lung, and cervix. Peutz-Jeghers syndrome is usually caused by mutations (changes) in the STK11 gene. Some people with Peutz-Jeghers syndrome do not have a mutation in the STK11 gene. In these cases, the cause of the disorder is unknown. Also called PJS.
| Identifier | MLC-T-ONC-006562 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | PJS |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-006562",
"term": "Peutz-Jeghers syndrome",
"field": "Oncology and biomedicine",
"definition": "A rare genetic disorder in which many polyps (abnormal growths of tissue) form in the lining of the gastrointestinal tract, and dark-colored spots appear on certain areas of the skin, such as around the mouth, eyes, and nose. People with Peutz-Jeghers syndrome have a very high risk of developing gastrointestinal cancer and other types of cancer, including cancers of the breast, pancreas, ovary, lung, and cervix. Peutz-Jeghers syndrome is usually caused by mutations (changes) in the STK11 gene. Some people with Peutz-Jeghers syndrome do not have a mutation in the STK11 gene. In these cases, the cause of the disorder is unknown. Also called PJS.",
"synonyms": [
"PJS"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/peutz-jeghers-syndrome/"
}
Record 13,049 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.