A complex case of MEN1

Naik, Dukhabandhu; Mahesh, D M; Asha, Hesarghatta Shyamasunder; Abraham, Deepak Thomas; Shanthly, Nylla; Chandramohan, Anuradha; Burad, Deepak; Ramakrishna, Banumathi; Paul, Mazhuvanchary Jacob; Kapoor, Nitin; Paul, Thomas M.; Chacko, Ari G; Thomas, Nihal

doi:10.1530/endoabs.38.p101

EJEA

2015

DOI: 10.1530/endoabs.38.p101

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A complex case of MEN1

Dukhabandhu Naik¹,

D M Mahesh²,

Hesarghatta Shyamasunder Asha³

et al.

Abstract: Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer syndrome, caused by germ line and somatic mutations in the tumour suppressor MEN-1 gene (11q13). MEN-1 is characterized by tumours of the parathyroid (83-97%), pancreas (38-84%), and anterior pituitary (18-65%).

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