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Pheochromocytoma and paraganglioma in patients with neurofibromatosis type 1

107

Citations

10

References

2016

Year

Abstract

We recommend patients with NF1 have biochemical case detection testing for PHEO/PGL every 3 years starting at age 10 to 14 years. Biochemical case detection testing should also be carried out prior to elective surgical procedures and conception.

References

YearCitations

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