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SAT-316 MAX-Related Bilateral Pheochromocytoma Associated with Subclinical Adrenal Insufficiency: A Case Report
INTRODUCTION: Loss-of-function mutation in the MYC-associated factor X (MAX) gene causes hereditary pheochromocytoma (PCC) that are frequently bilateral or multifocal(1). Adrenal insufficiency (AI) associated with unresected bilateral PCC has not been previously described. We hereby present a case o...
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| Publicado en: | J Endocr Soc |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Endocrine Society
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6552132/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SAT-316 |
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