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1 Σεπ 2012 · Patients with multiple endocrine neoplasia (MEN) type 1 (MEN1) and their families should be managed by a multidisciplinary team (MDT) consisting of relevant specialists with experience in the management of endocrine tumors (2|⊕⊕ ).
21 Οκτ 2022 · Multiple endocrine neoplasia type 1 (MEN1), also known as Wermer syndrome, is an autosomal dominant genetic disease that results in proliferative lesions in multiple endocrine organs, particularly the pituitary gland, pancreas, and parathyroid glands.
27 Σεπ 1999 · The endocrine disorders observed in multiple endocrine neoplasia type 2 (MEN2) are: medullary thyroid carcinoma (MTC) and/or its precursor, C-cell hyperplasia (CCH); pheochromocytoma; and parathyroid adenoma or hyperplasia.
Multiple endocrine neoplasias, or MEN for short, are a group of inherited diseases that cause tumors to grow in the endocrine glands of the body. MEN tumors are classified into two broad categories based on their underlying mutations.
20 Δεκ 2021 · Multiple endocrine neoplastic (MEN) syndromes are inherited disorders characterized by tumors in multiple endocrine glands. There are three main types: MEN1, MEN2a, and MEN2b. MEN1 is caused by mutations in the MEN1 gene and commonly involves the parathyroid, pancreas, and pituitary glands.
25 Φεβ 2022 · Multiple endocrine neoplasia, type 2A (MEN 2A) is an autosomal dominant syndrome characterized by medullary carcinoma of the thyroid, pheochromocytoma, parathyroid hyperplasia or adenomas (causing hyperparathyroidism), and occasionally cutaneous lichen amyloidosis.
10 Ιουλ 2023 · Multiple endocrine neoplasia type 1 (MEN1) is a rare endocrine tumor syndrome with high penetrance. This syndrome is also known as Wermer syndrome.[1] It primarily causes neoplasia of the parathyroid glands, the anterior pituitary gland, and the neuroendocrine tissue of gastro-entero-pancreatic organ systems.
