Autosomal dominant variants in the NF1 gene, located on chromosome 17q11.2, lead to diverse clinical manifestations, including café-au-lait macules, cutaneous neurofibromas, Lisch nodules, optic gliomas, seizures, pheochromocytomas, and osseous lesions [1]. Here, NF1 is linked to hereditary pheochromocytoma-paraganglioma.