Hyperinsulinaemic hypoglycaemia (HH) is a heterogeneous condition with dysregulated
insulin secretion which persists in the presence of low blood glucose levels. It is the most …

Purpose To retrospectively evaluate the age of onset of MEN1-associated lesions in a group
of affected children and adolescents and to compare the clinical features of our series with …

Although adult spontaneous (non-diabetic) hypoglycaemia is rare, its recognition is
important for the preventative or curative treatment of the underlying cause. Establishing …

Childhood adrenocortical carcinoma (ACC) is a rare disease that is mostly linked to familial
cancer syndrome. Although the prevalence of ACC is extremely low in children, it is clinically …

Purpose Multiple endocrine neoplasia types 1 (MEN1) and 2 (MEN2) are inherited
endocrine tumor syndromes caused by mutations in the MEN1 or RET genes. This study …

Background Insulinoma typically has non-specific neuroglycopenic symptoms. It is a
neuroendocrine tumor of the pancreas, and leads to recurring hypoglycemic attacks …

BACKGROUND: It is known that insulinoma in approximately 5% of cases is associated with
multiple endocrine neoplasia type 1 syndrome (MEN1), in which the prognosis and …

Аннотация Обоснование. Известно, что инсулинома приблизительно в 5% случаев
ассоциирована с синдромом множественных эндокринных неоплазий 1 типа (МЭН1) …

对1 例多发性内分泌腺瘤病1 型(multiple endocrine neoplasia type 1, MEN1)
合并低血糖昏迷的患者进行临床回顾性分析. 患者, 女性, 43 岁, 以反复低血糖为主要症状就诊 …

Abstract Background Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare autosomal
dominant disease that generally presents with primary hyperparathyroidism. However, initial …