Carcinoid syndrome causes: Difference between revisions
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==Overview== | ==Overview== | ||
Common causes of carcinoid syndrome include genetic disorders ([[multiple endocrine neoplasia type 1]] and [[neurofibromatosis type 1]]) and genetic mutations (gains involving chromosomes 5, 14, 17, and 19 and losses involving chromosomes 11 and 18). | Common causes of carcinoid syndrome include genetic disorders ([[multiple endocrine neoplasia type 1]] and [[neurofibromatosis type 1]]) and genetic mutations (gains involving chromosomes 5, 14, 17, and 19 and losses involving chromosomes 11 and 18). | ||
==Causes== | ==Causes== |
Revision as of 00:07, 5 January 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2]
Overview
Common causes of carcinoid syndrome include genetic disorders (multiple endocrine neoplasia type 1 and neurofibromatosis type 1) and genetic mutations (gains involving chromosomes 5, 14, 17, and 19 and losses involving chromosomes 11 and 18).
Causes
Common causes of carcinoid syndrome includes:[1]
- Genetic disorders
Genetic Disorder | Tumor Location |
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- Genetic mutations
Type of Mutation | Chromosomes |
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Gains |
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Losses |
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References
- ↑ Molecular genetics. National Cancer Institute. http://www.cancer.gov/types/gi-carcinoid-tumors/hp/gi-carcinoid-treatment-pdq