Guide To Endocrine System Diseases

Multiple Endocrine Neoplasia Type I

Multiple endocrine neoplasia type I, also known as Wermer's syndrome, is a rare inherited condition that affects an estimated one in every thirty thousand individuals. Patients with this condition have tumors in the duodenum and the endocrine glands. While the tumors are normally benign, they trigger the release of an excessive amount of hormones, which leads to illness. This condition is caused by genetic mutations, and symptoms may include bone pain, bone fractures, kidney stones, fatigue, and stomach ulcers. To diagnose multiple endocrine neoplasia type 1, doctors will perform a physical examination, blood tests, and imaging studies such as a CT or PET scan. There is no cure for multiple endocrine neoplasia type I at present, so treatment focuses on managing symptoms. If possible, surgery may be performed to remove tumors, and patients might have chemotherapy or radiation as well. Medications may be administered to control hormonal abnormalities.

Get more information on endocrine system diseases now.