Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C

• Main Authors: Sezer Acar (Author), Hale Tuhan (Author), Korcan Demir (Author), Ayça Aykut (Author), Asude Durmaz (Author), Ünal Utku Karaarslan (Author), Gözde İnci (Author), Oğuz Ateş (Author), Ece Böber (Author), Ayhan Abacı (Author)
• Format: Book
• Published: Galenos Yayinevi, 2018-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Pheochromocytoma is a rare disease that is characterized by the increased production and secretion of catecholamines from the adrenal medulla. The disease is autosomal dominant, and frequently sporadic and unilateral. Pheochromocytoma, which is diagnosed during childhood, mostly arises as a part of...