Endocrine Manifestations of Von Hippel–Landau Disease

Von Hippel–Lindau (VHL) disease is an autosomal dominant disorder characterized by various endocrine, nonendocrine, benign, and malignant tumors in various organs. VHL tumor suppressor gene, located on short arm of chromosome 3 is responsible for this. Pheochromocytoma (PCC) is one of the important...

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Detalles Bibliográficos
Autores principales: Pradhan, Roma, George, Nelson, Mandal, Kaushik, Agarwal, Amit, Gupta, Sushil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446673/
https://www.ncbi.nlm.nih.gov/pubmed/31016171
http://dx.doi.org/10.4103/ijem.IJEM_252_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446673/
https://www.ncbi.nlm.nih.gov/pubmed/31016171
http://dx.doi.org/10.4103/ijem.IJEM_252_18

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