MEN syndromes
a. Autosomal dominant inheritance with incomplete penetranceb. Characterized by hyperplasia and tumors of endocrine glands
2. MEN I (Werner syndrome)
a. Features tumors of the pituitary gland, parathyroids, and pancreasb. Associated with peptic ulcers and the Zollinger-Ellison syndrome
c. Genetic mutation of MEN I gene
MEN II (lla or Sipple syndrome)
a. Features medullary carcinoma of the thyroid, pheochromocytoma, and parathyroid
hyperplasia or adenoma
b. Genetic mutation of RET proto-oncogene
MEN III (lIb)
a. Features medullary carcinoma of the thyroid, pheochromocytoma, and mucocutaneous neuromas
b. Genetic mutation of RET proto-oncogene.
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