Inherited endocrine syndromes and MEN

Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)peer-review


This chapter begins with genetic testing for monogenic endocrine disorders, and then goes on to define the diagnosis, treatment, and management of McCune-Albright syndrome, neurofibromatosis, von Hippel-Lindau disease, Carney complex, Cowden syndrome, and POEMS syndrome. It then goes on to the clinical features and management of MEN type 1 and MEN type 2, and MEN type 4. Inherited primary hyperparathyroidism, phaeochromocytoma-paraganglioma syndromes, and renal calculi.
Original languageEnglish
Title of host publicationOxford handbook of endocrinology and diabetes
EditorsKatharine Owen, Helen Turner, John Wass
PublisherOxford University Press
Number of pages52
ISBN (Electronic)9780192594389
ISBN (Print)9780198851899
Publication statusPublished - Nov 2022


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