Inherited endocrine syndromes and MEN

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

Abstract

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
Chapter10
Pages651-702
Number of pages52
Edition4th
ISBN (Electronic)9780192594389
ISBN (Print)9780198851899
DOIs
Publication statusPublished - Nov 2022

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