Publication | Closed Access
Pheochromocytoma and paraganglioma in patients with neurofibromatosis type 1
107
Citations
10
References
2016
Year
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.
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