[HTML][HTML] Multiple endocrine neoplasia type 1 presenting with concurrent insulinoma and prolactinoma in early-adolescence
Y Akhtar, A Verardo, JL Crane - International Journal of Pediatric …, 2018 - Springer
Abstract Background Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare autosomal
dominant disease that generally presents with primary hyperparathyroidism. However, initial …
dominant disease that generally presents with primary hyperparathyroidism. However, initial …
Multifocal Insulinoma as the Unique Presenting Feature of MEN1 in an Adolescent
A Murray, SP Rodas Marquez… - Hormone Research in …, 2024 - karger.com
Multiple Endocrine Neoplasia Type 1 (MEN1) is an autosomal dominant inherited disorder
defined by the presence of two of the following endocrinopathies: primary …
defined by the presence of two of the following endocrinopathies: primary …
Multiple endocrine neoplasia type 1 familial case in a patient with insulinoma and primary hyperparathyroidism: First report in literature and in the Costa Rican …
P Molina‐Céspedes, EJ Ruiz‐Golcher… - Clinical Case …, 2023 - Wiley Online Library
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder without a
good genotype–phenotype correlation, characterized by tumor predisposition in the …
good genotype–phenotype correlation, characterized by tumor predisposition in the …
Multiple endocrine neoplasia type 1 with refractory hypoglycemia and lung and liver metastases: a case report
Y Wang, H Zhang - Journal of International Medical …, 2021 - journals.sagepub.com
Background Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant
genetic disease. MEN1 with multiple endocrine adenomatosis complicated by multiple …
genetic disease. MEN1 with multiple endocrine adenomatosis complicated by multiple …
[HTML][HTML] Multiple electrolyte disturbances as the presenting feature of multiple endocrine neoplasia type 1 (MEN-1)
APZ Li, S Sathyanarayan… - … & metabolism case …, 2022 - edm.bioscientifica.com
A 49-year-old teacher presented to his general physician with lethargy and lower limb
weakness. He had noticed polydipsia, polyuria, and had experienced weight loss, albeit with …
weakness. He had noticed polydipsia, polyuria, and had experienced weight loss, albeit with …
The early diagnosis of multiple endocrine neoplasia type 1 (MEN 1): a case report
G Tamagno, E De Carlo, C Martini, D Rubello… - Journal of …, 2004 - Springer
We report the case of a patient presenting amenorrhea, hyperprolactinemia, headache and
nuclear magnetic resonance (NMR) evidence of pituitary macroadenoma. The family history …
nuclear magnetic resonance (NMR) evidence of pituitary macroadenoma. The family history …
[HTML][HTML] Concomitant existence of pheochromocytoma in a patient with multiple endocrine neoplasia type 1
R Okada, T Shimura, S Tsukida, J Ando… - Surgical Case …, 2016 - Springer
Background Multiple endocrine neoplasia type 1 (MEN1) is an autosomal-dominant
inherited disorder that is classically characterized by the presence of neoplastic lesions of …
inherited disorder that is classically characterized by the presence of neoplastic lesions of …
A rare case of hypoglycaemia due to insulinoma in an adolescent with acutely altered mental status
KY Winston, J Dawrant - Journal of Pediatric Endocrinology and …, 2014 - degruyter.com
Background: Multiple endocrine neoplasia type 1 (MEN1) is an inherited neoplasia
syndrome that generally presents with hypercalcaemia due to hyperparathyroidism. Insulin …
syndrome that generally presents with hypercalcaemia due to hyperparathyroidism. Insulin …
Impact of Early Diagnostic and Therapeutic Interventions and Clinical Course in Children and Adolescents with Multiple Endocrine Neoplasia Types 1 and 2
JH Kim, Y Lee, S Hwang, JH Yoon… - Experimental and …, 2024 - thieme-connect.com
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 …
endocrine tumor syndromes caused by mutations in the MEN1 or RET genes. This study …
[HTML][HTML] Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer
syndrome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary …
syndrome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary …