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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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
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2021-10-01
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| Schriftenreihe: | Boletín Médico del Hospital Infantil de México |
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| Online-Zugang: | https://www.bmhim.com/frame_esp.php?id=216 |
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