Multiple endocrine neoplasia type 2 differential diagnosis
Multiple endocrine neoplasia type 2 Microchapters |
Differentiating Multiple endocrine neoplasia type 2 from other Diseases |
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Diagnosis |
Treatment |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Differential Diagnosis
Multiple endocrine neoplasia type 2 must be differentiated from following hereditary diseases.
Disease | Definition |
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Medullary thyroid carcinoma | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
C-cell hyperplasia | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Pheochromocytoma | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
VHL (von Hippel Lindau) syndrome | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Hereditary paraganglioma-pheochromocytoma syndrome | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Polycythemia and paraganglioma/pheochromocytoma | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Neurofibromatosis type 1 | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Multiple endocrine neoplasia type 4 (MEN 4) | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |
Multiple endocrine neoplasia type 1 (MEN 1) | An autosomal dominant genetic disorder causing abnormal growth of blood vessels in different parts of the body. |