Von Hippel-Lindau Disease: A Rare Radiological Case Report of a Symptomatic Patient and His Asymptomatic Genetic Counterpart

Von Hippel-Lindau (VHL) disease is an inherited syndrome manifested as a benign and malignant tumor. It is an autosomal dominant syndrome diagnosed approximately in 1 in 36,000 people. We report a case where male siblings presented with the involvement of bilateral kidneys and the multi-cystic lesio...

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Detalles Bibliográficos
Autores principales: Khanduri, Sachin, Khan, Nazia, Malik, Saif, Katara, Shivangi, Fatima, Mariyam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Family/General Practice
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906916/
https://www.ncbi.nlm.nih.gov/pubmed/33654607
http://dx.doi.org/10.7759/cureus.12925

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906916/
https://www.ncbi.nlm.nih.gov/pubmed/33654607
http://dx.doi.org/10.7759/cureus.12925

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