Lecturio Medical - The MEN-2 syndrome is also inherited autosomal dominantly and can further be divided into the Sipple's syndrome (2a), the Gorlin's syndrome (2b) and the FMTC-only (familial medullary thyroid carcinoma).
Endocrines | Free Full-Text | Involvement of the MEN1 Gene in Hormone-Related Cancers: Clues from Molecular Studies, Mouse Models, and Patient Investigations
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Types of MEN (Multiple Endocrine Neoplasia) Syndromes
The UnExplainer - MEN 1 or Wermer Syndrome 1. Parathyroid hyperplasia (~80%) 2. Pituitary adenoma (~66%) 3. Pancreatic tumours (e.g. Gastrinoma [50%], insulinoma) Gene =MEN1 gene, menin protein (tumour suppressor) MEN 2a