Von Hippel-Lindau Disease: A New Approach to an Old Problem | Zendy

Ali Tootee | Zendy; Shirin Hasani Ranjbar | Zendy

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Von Hippel-Lindau Disease: A New Approach to an Old Problem

Author(s) -

Ali Tootee,

Shirin Hasani Ranjbar

Publication year - 2012

Publication title -

international journal of endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.652

H-Index - 23

eISSN - 1726-9148

pISSN - 1726-913X

DOI - 10.5812/ijem.4510

Subject(s) - medicine , von hippel–lindau disease , disease , hemangioblastoma , pheochromocytoma , referral , pediatrics , intensive care medicine , pathology , bioinformatics , family medicine , biology

Von Hippel-Lindau (VHL) disease is a hereditary, autosomal dominant syndrome which is manifested by a range of different benign and malignant tumors. This disease can present with different clinical presentations such as; retinal angioma (RA), hemangioblastoma (HB) of the central nervous system (CNS), pheochromocytoma (Pheo), and epididymal cystadenoma. Tumors are usually accompanied with cysts.

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