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A case of pheochromocytoma presenting as syncope due to long QT syndrome
Article | IMSEAR | ID: sea-193948
Pheochromocytoma, a catecholamine secreting tumour, is rare and we are presenting such a case who presened with syncopal episodes due to arrhythmias associated with the tumour. The patient was managed with pharmacologic and surgical treatment.
Texto completo: 1 Índice: IMSEAR Año: 2018 Tipo del documento: Article
Texto completo: 1 Índice: IMSEAR Año: 2018 Tipo del documento: Article