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Significados de multiple endocrine neoplasia type i en inglés

ruso
синдром вермера
portugués
neoplasia endócrina múltipla do tipo 1
catalán
neoplàsia endocrina múltiple tipus 1
español
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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Términos relacionados
neoplasia endocrina múltiple tipo 1
Sinónimos
Examples for "men type i"
Examples for "men type i"
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The men 1ining the hall watch with casual interest.
Miller's crossing
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The men 1 gene has been mapped by genetic studies to the long arm of human chromosome 11, region q12-13.
Pubmed
3
Genetic analysis of families and tumoral deletion mapping made possible to narrow the men 1 region to a 5 cM interval on chromosome 11q12-13.
Pubmed
4
No clinical, laboratory, or MEN 1 feature distinguished patients with meningiomas.
Pubmed
5
North American Climbing Championships Lead Climbing Final Men 1.
Climbing Magazine
1
Three patients had atypical carcinoids, one with multiple endocrine neoplasia type 1 syndrome.
Pubmed
2
Eight patients had sporadic NETs, and 1 had multiple endocrine neoplasia type 1 syndrome.
Pubmed
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
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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
1
Conclusions: Unlike some other syndromes where a genetic mutation can predict clinical course, there is no genotype-phenotype correlation in MEN1 syndrome.
Pubmed
2
However, the coexistence of MEN1 syndrome and malignant tumor such as low-grade fibromyxoid sarcoma has not been described in the literature.
Pubmed
3
The patient with Zollinger-Ellison and MEN1 syndrome has been followed 3 years after diagnosis and 2 years after total gastrectomy.
Pubmed
4
We describe a young woman who fulfilled the clinical and biochemical criteria for MEN1 syndrome, but DNA sequencing did not indicate any MEN1 mutations.
Pubmed
Uso de multiple endocrine neoplasia type i en inglés
1
At diagnosis, all patients were checked for the presence of multiple endocrine neoplasia type I syndrome.
Pubmed
Translations for multiple endocrine neoplasia type i