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Pheochromocytoma in a 2.75-year-old-girl with a germline von Hippel–Lindau mutation Q164R

✍ Scribed by Petra Sovinz; Christian Urban; Sabine Uhrig; Vinzenz Stepan; Herwig Lackner; Wolfgang Schwinger; Martin Benesch; Andrea Moser; Ekkehard Spuller; Michael R. Speicher

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
157 KB
Volume
152A
Category
Article
ISSN
1552-4825

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✍ 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