Open AccessSAT-324 An Unusual Association between Pheochromocytoma and Hyperparathyroidism in a Patient with Neurofibromatosis Type 1: A Possible Co-Occurrence of Two Hereditary Endocrine Tumor Syndromes
Author(s) -
Phatharaporn Kiatpanabhikul,
Natnicha Houngngam,
Thachanun Porntharukchareon,
Thiti Snabboon
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-sat-324
Subject(s) - medicine , pheochromocytoma , multiple endocrine neoplasia , neurofibromatosis , hyperparathyroidism , multiple endocrine neoplasia type 2 , metanephrines , parathyroid adenoma , parathyroidectomy , thyroid , parathyroid gland , endocrinology , pathology , gastroenterology , parathyroid hormone , germline mutation , gene , biochemistry , chemistry , mutation , calcium
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