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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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| Published in: | Indian J Endocrinol Metab |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Wolters Kluwer - Medknow
2019
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| Subjects: | |
| Online Access: | 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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