Searchable abstracts of presentations at key conferences in endocrinology

ea0099rc2.5 | Rapid Communications 2: Calcium and Bone | Part I | ECE2024

Genetic testing for syndromic conditions in patients referred with primary hyperparathyroidism: a retrospective observational analysis

Than Yu Kyi Pyar , Gregory Andrew , Abdulkareem Mustafa , Jose Biju , Varadhan Lakshminarayanan

Background and Aim: Primary hyperparathyroidism (PHPT) is a common endocrine disorder. A small proportion of these patients may have syndromic conditions such as multiple endocrine neoplasia (MEN) or familial hypocalciuric hypercalcemia (FHH). The UK national guidelines recommend genetic testing for familial hyperparathyroidism in individuals under 50 or any age with specific criteria such as family history, multi glandular disease, hyperplasia, or parathyroid carcinoma. Genet...