Bilateral Pheochromocytomas in a Patient with Y175C Von Hippel-Lindau Mutation

Von Hippel-Lindau (VHL) disease, caused by germline mutations in the VHL gene, is characterized by metachronously occurring tumors including pheochromocytoma, renal cell carcinoma (RCC), and hemangioblastoma. Although VHL disease leads to reduced life expectancy, its diagnosis is often missed and tu...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Case Rep Endocrinol
Asıl Yazarlar: Astapova, Olga, Biswas, Anindita, DiMauro, Alessandra, Moalem, Jacob, Hammes, Stephen R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2018
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6076969/
https://ncbi.nlm.nih.gov/pubmed/30105105
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/8967159
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller