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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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Dettagli Bibliografici
Pubblicato in:Indian J Endocrinol Metab
Autori principali: Pradhan, Roma, George, Nelson, Mandal, Kaushik, Agarwal, Amit, Gupta, Sushil K.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Wolters Kluwer - Medknow 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6446673/
https://ncbi.nlm.nih.gov/pubmed/31016171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijem.IJEM_252_18
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