SULT2A1 and hereditary pheochromocytoma-paraganglioma: Adrenal myelolipomas are found to occur concurrently with other conditions with hormonal dysfunction such as cortical adenoma [21], ganglioneuroma [22], carcinoma [23], pheochromocytoma [24], Cushing's and Conn's syndrome [25], overproduction of dehydroepiandrosterone sulphate (DHEAS), and CAH due to 21 hydroxylase deficiency or 17 α-hydroxylase deficiency [26, 27].