Multiple endokrine Neoplasie
Multiple endocrine neoplasia (MEN) syndromes are a collection of syndromes characterized by the presence of, as the name would suggest, multiple endocrine tumors. They are autosomal dominant in inheritance.
- MEN1 (Wermer syndrome)
- MEN2 (multiple endocrine adenomatosis)
- MEN2a (Sipple syndrome)
- MEN2b (previously known as MEN3 )
- familial medullary thyroid carcinoma
- MEN4
- Carney complex
Siehe auch:
und weiter:
Assoziationen und Differentialdiagnosen zu Multiple endokrine Neoplasie:
