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 language | English |
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Title of host publication | Oxford handbook of endocrinology and diabetes |
Editors | Katharine Owen, Helen Turner, John Wass |
Publisher | Oxford University Press |
Chapter | 10 |
Pages | 651-702 |
Number of pages | 52 |
Edition | 4th |
ISBN (Electronic) | 9780192594389 |
ISBN (Print) | 9780198851899 |
DOIs | |
Publication status | Published - Nov 2022 |