Multiple endocrine neoplasia type 2 syndrome
| Multiple endocrine neoplasia type 2 syndrome | |
|---|---|
| Term | Multiple endocrine neoplasia type 2 syndrome |
| Short definition | Multiple endocrine neoplasia type 2 syndrome - (pronounced) (MUL-tih-pul EN-doh-krin NEE-oh-PLAY-zhuh . |
| Type | Cancer terms |
| Specialty | Oncology |
| Language | English |
| Source | NCI |
| Comments | |
Multiple endocrine neoplasia type 2 syndrome - (pronounced) (MUL-tih-pul EN-doh-krin NEE-oh-PLAY-zhuh . . . SIN-drome) rare genetic disorder that affects the endocrine glands and can cause tumors in the thyroid, parathyroid, and adrenal glands. The affected endocrine glands can produce high levels of hormones, which can lead to other medical problems like high blood pressure and kidney stones. Multiple endocrine neoplasia type 2 syndrome is caused by a mutation (change) in a gene called RET and is divided into three subtypes (MEN2A, MEN2B and FMTC). People with all subtypes of type 2 syndrome multiple endocrine neoplasia have an increased risk of medullary thyroid cancer, pheochromocytoma, and parathyroid cancer. Also called MEN2, MEN2 syndrome and multiple endocrine adenomatosis type 2
External links
- Medical encyclopedia article on Multiple endocrine neoplasia type 2 syndrome
- Wikipedia's article - Multiple endocrine neoplasia type 2 syndrome
This WikiMD dictionary article is a stub. You can help make it a full article.
Languages: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
Urdu,
বাংলা,
తెలుగు,
தமிழ்,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
European
español,
Deutsch,
français,
русский,
português do Brasil,
Italian,
polski