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- Jane E McDonnell, Matti L Gild, Roderick J Clifton-Bligh, and Bruce G Robinson.
- Department of Endocrinology and Diabetes, Royal North Shore Hospital, Sydney, New South Wales, Australia.
- Intern Med J. 2019 Aug 1; 49 (8): 954-961.
AbstractThe multiple endocrine neoplasia (MEN) syndromes include MEN1, MEN2 (formerly MEN2A), MEN3 (formerly MEN2B) and the recently identified MEN4. Clinical presentations are varied and often relate to the overproduction of specific hormones. Understanding the genetics of each syndrome assists in determining screening timelines. Treatments for each manifestation are dependent on location, risk of recurrence or malignancy, hormone excess and surgical morbidity. Multidisciplinary management should include geneticists, genetic counsellors, endocrinologists and endocrine surgeons.© 2019 Royal Australasian College of Physicians.
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