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Asymptomatic phaeochromocytoma in a patient with Holt-Oram syndrome: a case report
BACKGROUND: Holt-Oram syndrome (HOS) is a rare congenital disease that affects the heart and upper limbs. Phaeochromocytoma, a catecholamine-secreting tumour, is a rare neuroendocrine disorder. We present an interesting case presentation of these two rare disorders in a patient who was asymptomatic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026609/ https://www.ncbi.nlm.nih.gov/pubmed/32099963 http://dx.doi.org/10.1093/ehjcr/ytz206 |