Multiple endocrine neoplasia type 2 screening: Difference between revisions
(Created page with "__NOTOC__ {{Multiple endocrine neoplasia type 2}} {{CMG}}; {{AE}} {{Ammu}} ==Overview== ==Screening== * RET gene testing for children with increased risk of Multiple endocrine...") |
No edit summary |
||
Line 3: | Line 3: | ||
{{CMG}}; {{AE}} {{Ammu}} | {{CMG}}; {{AE}} {{Ammu}} | ||
==Overview== | ==Overview== | ||
According to the [guideline name], screening for multiple endocrine neoplasia type 2 by ''RET'' gene testing is recommended for children with increased risk of Multiple endocrine neoplasia type 2 with increased risk of Multiple endocrine neoplasia type 2. | |||
==Screening== | ==Screening== | ||
* RET gene testing for children with increased risk of Multiple endocrine neoplasia type 2. | * RET gene testing for children with increased risk of Multiple endocrine neoplasia type 2. |
Revision as of 20:15, 25 September 2015
Multiple endocrine neoplasia type 2 Microchapters |
Differentiating Multiple endocrine neoplasia type 2 from other Diseases |
---|
Diagnosis |
Treatment |
Multiple endocrine neoplasia type 2 screening On the Web |
American Roentgen Ray Society Images of Multiple endocrine neoplasia type 2 screening |
Directions to Hospitals Treating Multiple endocrine neoplasia type 2 |
Risk calculators and risk factors for Multiple endocrine neoplasia type 2 screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
According to the [guideline name], screening for multiple endocrine neoplasia type 2 by RET gene testing is recommended for children with increased risk of Multiple endocrine neoplasia type 2 with increased risk of Multiple endocrine neoplasia type 2.
Screening
- RET gene testing for children with increased risk of Multiple endocrine neoplasia type 2.
- Ionized calcium level yearly for MEN 2A
- Parathyroid hormone level yearly for MEN 2A
- Catacholamines, epinephrine and norepinephrine yearly for MEN 2A and MEN 2B
- Magnetic resonance imaging and computerized tomography for pheochromocytoma every 2-4 years