Clinical case: multiple endocrine neoplasia type 1 (MEN 1)

Clinical case: multiple endocrine neoplasia type 1 (MEN 1)

Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations...

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Format: Article
Language:English
Published: Endocrinology Research Centre 2012-12-01
Series:Ожирение и метаболизм
Subjects:
синдром Вермера
МЭН 1
пролактинома
пролактин
гиперпаратиреоз
инсулинома
проинсулин
Online Access:https://endojournals.ru/index.php/omet/article/view/5129
id doaj-6a39601c34e147fdb5657d9bf386f60c
record_format Article
spelling doaj-6a39601c34e147fdb5657d9bf386f60c2021-10-02T15:52:22ZengEndocrinology Research CentreОжирение и метаболизм2071-87132306-55242012-12-0194444710.14341/2071-8713-51295087Clinical case: multiple endocrine neoplasia type 1 (MEN 1)Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations have been described. This case demonstrates multiple formations of endocrine organs, starting non-classical with macroprolactonoma resistant to dopamine agonists therapy, other endocrine disorders developed gradually eventually: hyperparathyreoidism and hypoglycemia caused by pancreas lesions, produced proinsulin in high levels.https://endojournals.ru/index.php/omet/article/view/5129синдром ВермераМЭН 1пролактиномапролактингиперпаратиреозинсулиномапроинсулин
collection DOAJ
language English
format Article
sources DOAJ
title Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
spellingShingle Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
Ожирение и метаболизм
синдром Вермера
МЭН 1
пролактинома
пролактин
гиперпаратиреоз
инсулинома
проинсулин
title_short Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
title_full Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
title_fullStr Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
title_full_unstemmed Clinical case: multiple endocrine neoplasia type 1 (MEN 1)
title_sort clinical case: multiple endocrine neoplasia type 1 (men 1)
publisher Endocrinology Research Centre
series Ожирение и метаболизм
issn 2071-8713
2306-5524
publishDate 2012-12-01
description Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer syndrome) – group o а heterogeneous inherited deseases, caused by hyperlasia or neoplasia of several endocrine glands. The phenotype of MEN1 is broad, and over 20 different combinations of endocrine and non-endocrine metabolic manifestations have been described. This case demonstrates multiple formations of endocrine organs, starting non-classical with macroprolactonoma resistant to dopamine agonists therapy, other endocrine disorders developed gradually eventually: hyperparathyreoidism and hypoglycemia caused by pancreas lesions, produced proinsulin in high levels.
topic синдром Вермера
МЭН 1
пролактинома
пролактин
гиперпаратиреоз
инсулинома
проинсулин
url https://endojournals.ru/index.php/omet/article/view/5129
_version_ 1716852883311296512

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