Von-Hipple Lindau syndrome with family history: a case report and seventeen years follow-up study

ConclusionThe clinical presentation of VHL syndrome is atypical, and early identification and treatment of VHL syndrome is possible by genetic testing techniques. Multiple relapses occurred during the course of the disease, but early diagnosis and aggressive treatment allowed the patients to survive well.
Source: Frontiers in Oncology - Category: Cancer & Oncology Source Type: research