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. 2018 Feb 10;55(4):254–260. doi: 10.1136/jmedgenet-2017-104957

Table 1.

Clinical characteristics of the whole cohort

Clinical characteristic n=1405*
AIP mutation, n (%) 134 (9.5)
Familial, n (%) 607 (43.2)
Gender, n (% male) 680 (48.5)
Diagnosis, n (%)
 GH excess 767 (55.5)
 NFPA 185 (13.4)
 Prolactinoma 344 (24.9)
 Cushing’s disease 74 (5.4)
 Other diagnosis 11 (0.8)
Age of onset (years) 27.1±13.1
Age at diagnosis (years) 30.8±13.4
Macroadenoma, n (%) 977 (81.5)
Extrasellar extension, n (%) 446 (60.1)
Pituitary apoplexy, n (%) 48 (3.9)

*Prospectively diagnosed patients excluded.

NFPA, non-functioning pituitary adenoma.