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

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...

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Detalhes bibliográficos

Principais autores:	Paulina M. Núñez-Martínez, Lucía Taja-Chayeb, Miguel A. Ramírez-Otero, Verónica Fragoso-Ontiveros, Talia Wegman-Ostrosky, David Cruz-Robles, Silvia Vidal-Millán
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Permanyer 2021-10-01
Colecção:	Boletín Médico del Hospital Infantil de México
Assuntos:	von Hippel-Lindau Disease. Chuvash polycythemia. VHL gene. Hereditary cancer syndrome. Familial erythrocytosis type 2. Polyglobulia.
Acesso em linha:	https://www.bmhim.com/frame_esp.php?id=216
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