Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep608 | Endocrine-Related Cancer | ECE2022

Clinical case: MEN1 syndrome

Meskinyte Ieva , Cyrolyte Saule , Strazdiene Igne , Urbonaviciute Egle , Klimaite Raimonda , Jakubonienė Neli

Introduction: Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare, autosomal dominantly inherited syndrome that causes tumors of the endocrine glands [1]. This syndrome is most commonly associated with neuroendocrine tumors of the parathyroid glands, pituitary gland and pancreas [2].Case: A 30-year-old woman was admitted to the Hospital of Lithuanian University of Health Sciences, Kaunas Clinics for unconsciousness and significant hypoglycaemia: 1.0 - 3...