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...
Format: | Article |
---|---|
Language: | English |
Published: |
Endocrinology Research Centre
2012-12-01
|
Series: | Ожирение и метаболизм |
Subjects: | |
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 |