Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

• Main Authors: Paulina M. Núñez-Martínez (Author), Lucía Taja-Chayeb (Author), Miguel A. Ramírez-Otero (Author), Verónica Fragoso-Ontiveros (Author), Talia Wegman-Ostrosky (Author), David Cruz-Robles (Author), Silvia Vidal-Millán (Author)
• Format: Book
• Published: Permanyer, 2021-10-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Background: Patients with familial erythrocytosis type 2 have no increased risk of von Hippel-Lindau-associated tumors, although mutations in the VHL gene cause both pathologies. Case report: We present a case of a compound heterozygote patient with von Hippel-Lindau disease and familial erythrocyto...