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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| Main Authors: | , , , , , , |
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| Format: | Book |
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Permanyer,
2021-10-01T00:00:00Z.
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