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

✍ Scribed by Jennifer MJ Schreinemakers; Bernard A Zonnenberg; Jo WM Höppener; Frederik J Hes; Inne HM Borel Rinkes; Cornelis JM Lips


Book ID
119903436
Publisher
BioMed Central
Year
2007
Tongue
English
Weight
495 KB
Volume
5
Category
Article
ISSN
1477-7819

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Genotype–phenotype correlations of pheoc
✍ Sarah M. Nielsen; Wendy S. Rubinstein; Darcy L. Thull; Michaele J. Armstrong; El 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 129 KB 👁 2 views

## Abstract Von Hippel–Lindau (VHL) disease type 2A is an inherited tumor syndrome characterized by predisposition to pheochromocytoma (pheo), retinal hemangioma (RA), and central nervous system hemangioblastoma (HB). Specific VHL subtypes display genotype–phenotype correlations but, unlike other f