2024年10月4日 · Multiple endocrine neoplasia, type 1 (MEN 1) is a rare condition. It mainly causes tumors in the glands that make and release hormones. These are called the endocrine glands. The condition also can cause tumors in the small intestine and stomach. Another name for MEN 1 is Wermer's syndrome.

Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic disorder that mainly affects the endocrine glands. Located in different parts of the body, these glands control the production of hormones that direct many body processes, including growth, digestion, and sexual function.

Multiple endocrine neoplasia type 1 (MEN-1 aka Wermer Syndrome) is one of a group of disorders, the multiple endocrine neoplasias, that affect the endocrine system through development of neoplastic lesions in pituitary, parathyroid gland and pancreas. [1] .

2022年5月23日 · There are two main types of the condition: Multiple endocrine neoplasia (MEN) type 1: This is a genetic condition in which multiple tumors affect different aspects of your endocrine system. Multiple endocrine neoplasia type 2 (MEN2): This is a genetic polyglandular (multiple glands) cancer syndrome.

2024年10月4日 · To find out if you have multiple endocrine neoplasia, type 1 (MEN 1), your healthcare professional starts by doing a physical exam. You also answer questions about your health history and family history. You may have a blood test and imaging tests, including the following: Magnetic resonance imaging (MRI).

2023年7月10日 · Multiple endocrine neoplasia type 1 (MEN1) is a rare endocrine tumor syndrome with high penetrance. This syndrome is also known as Wermer syndrome. It primarily causes neoplasia of the parathyroid glands, the anterior pituitary gland, and the neuroendocrine tissue of gastro-entero-pancreatic organ systems.

Multiple endocrine neoplasia type 1 is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing.

Multiple endocrine neoplasia type 1 (MEN1) is a genetic condition that causes benign and malignant tumors in endocrine (hormone producing) and non-endocrine tissues. It occurs in approximately 1 in 30,000 individuals.

Multiple endocrine neoplasia, type 1 (MEN 1) is an autosomal dominant syndrome characterized by hyperplasia or adenomas of the parathyroid glands, pancreatic islet cell tumors (also known as pancreatic neuroendocrine tumors), and/or pituitary gland tumors.

What is multiple endocrine neoplasia type 1 (MEN1)? MEN1 is an inherited disorder that causes tumors in the endocrine glands and the duo­ denum, the irst part of the small intestine. MEN1 is sometimes called multiple endo­ crine adenomatosis or Wermer’s syndrome, after one of the irst doctors to recognize it.