Multiple endocrine neoplasia: an update
Copyright policy )Multiple endocrine neoplasia: an update
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.
- Kolling Institute of Medical Research Australia
- University of Sydney Australia
- Royal North Shore Hospital Australia
Genetic Markers, Recurrence, Endocrine Surgical Procedures, Multiple Endocrine Neoplasia, Humans, Genetic Testing, Combined Modality Therapy
Genetic Markers, Recurrence, Endocrine Surgical Procedures, Multiple Endocrine Neoplasia, Humans, Genetic Testing, Combined Modality Therapy
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