ea0005p114 | Endocrine Tumours and Neoplasia | BES2003
Turner J
, Pannett A
, Kennedy A
, Forbes S
, Cavaco B
, Bassett J
, Cianferotti L
, Harding B
, Shine B
, Flinter F
, Maidment C
, Trembath R
, Thakker R
Primary hyperparathyroidism (HPT) is most frequently encountered as a non-familial disorder, but 10% of patients with primary HPT will have a hereditary form, which may occur as an isolated endocrinopathy or as part of a complex tumour syndrome such as multiple endocrine neoplasia type 1 (MEN 1) or type 2 (MEN 2), or the hereditary hyperparathyroidism-jaw tumour syndrome (HPT-JT). Familial isolated hyperparathyroidism (FIHP) is an autosomal dominant disorder characterised by u...