MEN Syndromes
MEN 1 – Autosomal dominant, affected gene: menin
Pancreatic tumours (only in MEN-1)
Pituitary adenomas
Parathyroid hyperplasia
MEN 2
2a: Parathyroid hyperplasia
Medullary thyroid ca (raised calcitonin)
Phaeochromocytoma (only in MEN-2A)
2b: Medullary thyroid ca
Marfanoid body habitus
Mucosal neuromata