Purpose This article reports on a 12-year follow-up of a Colombian family with a novel MEN1
gene variant (c. 698dup, p. Met233IlefsTer4), identified through cascade genetic screening …

Background Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant
disorder marked by pathogenic variants in the MEN1 tumor suppressor gene, leading to …

Multiple endocrine neoplasia type 1 (MEN1) is a hereditary endocrine tumor syndrome
caused by pathogenic variants in the MEN1 gene, and most patients with this syndrome …

Background Multiple endocrine neoplasia type 1 (MEN1) is a hereditary cancer syndrome
associated with several endocrine as well as non-endocrine tumors and is caused by …

A 38-year-old female was identified as carrying a heterozygous pathogenic MEN1 variant (c.
1304delG) through predictive genetic testing, following a diagnosis of familial …

A 41-year-old Caucasian male has been followed over the past two decades in an
endocrine clinic. At the age of 21, he was found to have adenoma of the right superior …

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder without a
good genotype–phenotype correlation, characterized by tumor predisposition in the …

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor
syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) …

Materials and Methods A 64-year-old man, referred to our gastroenterology outpatient clinic
for evaluation of a pancreatic mass lesion, was diagnosed with MEN1 syndrome after …

Background Multiple endocrine neoplasia type 1 (MEN1) syndrome is an autosomal
dominant hereditary disorder characterized by the presence of endocrine tumors affecting …