Transmissible genes induced chromosome-type aberrations in the lymphocytes of multiple endocrine neoplasia type 1 and type 2A (MEN1 and MEN2A) patients

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Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)

Multiple endocrine neoplasia (MEN) is characterized by the occurrence of tumors involving two or more endocrine glands within a single patient. Four major forms of MEN, which are autosomal dominant disorders, are recognized and referred to as: MEN type 1 (MEN1), due to menin mutations; MEN2 (previously MEN2A) due to mutations of a tyrosine kinase receptor encoded by the rearranged during transf...

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Diagnosis and Management of Multiple Endocrine Neoplasia Type 1 (MEN1)

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited disorder, characterised by the occurrence of tumours of the parathyroid glands, the pancreatic islets, the pituitary gland, the adrenal glands and neuroendocrine carcinoid tumours. Carcinoid tumours of the thymus and pancreatic-duodenal gastrinomas are the most harmful tumour types, since these tumours have malignan...

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Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

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Multiple endocrine neoplasia type 2A (MEN2A), a subtype of MEN2, is characterized by medullary thyroid cancer, pheochromocytoma, and primary hyperparathyroidism. A Han Chinese pedigree with MEN2A was investigated following confirmation of the proband's diagnosis by pathological findings and DNA/biochemical screening. DNA samples from 4 other family members were collected and exon 5, 8, 10, 11, ...

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ژورنال

عنوان ژورنال: Indian Journal of Science and Technology

سال: 2010

ISSN: 0974-6846,0974-5645

DOI: 10.17485/ijst/2010/v3i9.4