Searchable abstracts of presentations at key conferences in endocrinology

ea0019p171 | Endocrine tumours and neoplasia | SFEBES2009

Asymptomatic children with multiple endocrine neoplasia type 1 (MEN1) mutations harbour pancreatic and pituitary tumours

Newey P , Jeyabalan J , Christie P , Shine B , Phillips R , Gleeson F , Gould S , Soonawalla Z , Johnson P , Ryan F , Thakker R

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by parathyroid, anterior pituitary and pancreatic islet tumours. Primary hyperparathyroidism is the first clinical manifestation in >85% of patients, although in some patients pancreatic and pituitary tumours may precede the occurrence of primary hyperparathyroidism. The earliest occurrence of MEN1-tumours has been reported at the age of 5 years following which the age-related penetr...