Hereditary paraganglioma-pheochromocytoma syndromes associated with SDHD and RET mutations
Background. Hereditary paraganglioma-pheochromocytoma syndromes (PGL/PCC) are rare tumors arising from neuroendocrine cells. Methods and Results. The proband, a 59-year-old white man and his 42-year-old elder son had a medical history of bilateral carotid body PGL and both presented for treatment of abdominal PGLs. His 36-year-old daughter had excision of recurrent malignant carotid body PGL and vertebral metastasis. His 33-year-old youngest son presented for excision of a unilateral carotid...[Show more]
|Collections||ANU Research Publications|
|Source:||Head and Neck|
|01_Choi_Hereditary_2014.pdf||90.64 kB||Adobe PDF||Request a copy|
|02_Choi_Hereditary_2014.pdf||91.47 kB||Adobe PDF||Request a copy|
Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.