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...

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Detalles Bibliográficos
Autores principales: Ng, Perryn, Deepak, Doddabele, Teo, Lynette, Low, Ting Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Case Reports
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

Internet

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

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