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Значения термина multiple endocrine neoplasia type 1 на английском

русский
синдром вермера
португальский
neoplasia endócrina múltipla do tipo 1
каталонский
neoplàsia endocrina múltiple tipus 1
испанский
neoplasia endocrina múltiple tipo 1

Autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas.

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Использование термина multiple endocrine neoplasia type 1 на английском
1
Three patients had atypical carcinoids, one with multiple endocrine neoplasia type 1 syndrome.
Pubmed
2
Pituitary adenomas represent one of the key features of multiple endocrine neoplasia type 1.
Pubmed
3
She was diagnosed as having multiple endocrine neoplasia type 1 with gastrinoma and liver metastases.
Pubmed
4
Eight patients had sporadic NETs, and 1 had multiple endocrine neoplasia type 1 syndrome.
Pubmed
5
An association between blood type O and neuroendocrine tumors in multiple endocrine neoplasia type 1 (MEN1) patients was recently suggested.
Pubmed
6
Inactivating mutations in the MEN1 gene predisposing to the multiple endocrine neoplasia type 1 (MEN1) syndrome can also cause sporadic pancreatic endocrine tumors.
Pubmed
7
The lesion in the upper mediastinum was subsequently proven pathologically as parathyroid hyperplasia in a patient with multiple endocrine neoplasia type 1 (MEN-1 syndrome).
Pubmed
8
Multiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the MEN1 gene on chromosome 11.
Pubmed
9
Multiple endocrine neoplasia type 1 (MEN1) is an inherited syndrome characterized by development of multiple endocrine tumors in affected individuals.
Pubmed
Translations for multiple endocrine neoplasia type 1