PHTS
PHTS | |
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Term | PHTS |
Short definition | PHTS - A group of inherited diseases caused by mutations (changes) in the PTEN gene. In people with PHTS, many benign (noncancerous) growths called hamartomas form in various parts of the body, particularly the skin, mouth, and gastrointestinal tract. |
Type | Cancer terms |
Specialty | Oncology |
Language | English |
Source | NCI |
Comments |
PHTS - A group of inherited diseases caused by mutations (changes) in the PTEN gene. In people with PHTS, many benign (noncancerous) growths called hamartomas form in various parts of the body, particularly the skin, mouth, and gastrointestinal tract. Benign tumors can also occur in the thyroid, breast, uterus, soft tissues, and brain. Other signs and symptoms include a head that is larger than average, abnormal skin changes, blood vessel problems, autism spectrum disorders, and learning and developmental delays. People with PHTS have an increased risk of developing certain types of cancer, including melanoma and breast, thyroid, kidney, endometrial, colon, and rectal cancer. Also known as PTEN hamartoma tumor syndrome
External links
- Medical encyclopedia article on PHTS
- Wikipedia's article - PHTS
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