A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C

BACKGROUND: Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited disease. It is relatively recent that type 2C was identified as a separate group solely presenting with pheochromocytomas. As an illustration, an interesting case is presented of a pregnant woman with refractory hypertens...

Descripción completa

Detalles Bibliográficos
Autores principales: Schreinemakers, Jennifer MJ, Zonnenberg, Bernard A, Höppener, Jo WM, Hes, Frederik J, Rinkes, Inne HM Borel, Lips, Cornelis JM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169240/
https://www.ncbi.nlm.nih.gov/pubmed/17922902
http://dx.doi.org/10.1186/1477-7819-5-112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169240/
https://www.ncbi.nlm.nih.gov/pubmed/17922902
http://dx.doi.org/10.1186/1477-7819-5-112

Ejemplares similares