Table 1 Hereditary conditions associated with pheochromocytomas and paragangliomas

MEN 2A and 2B

10q11.2

RET mutation

Von Hippel–Lindau

3p26-29

VHL mutation

Neurofibromatosis I

17q11.2

NF1 mutation

Familial PGL1

11q23

SDHD mutation

Familial PGL2

11q13.1

SDHAF2 mutation

Familial PGL3

1q2

SDHC mutation

Familial PGL4

1q23-25

SDHB mutation