We report clinicopathologic features of a case of von Hippel-Lindau disease in a patient who had been clinically followed for bilateral retinal and cerebellar involvement. Two of the patient's retinal hemangiomas appeared to show evidence of spontaneous regression.
|Original language||English (US)|
|Number of pages||7|
|Publication status||Published - 1986|
ASJC Scopus subject areas
- Sensory Systems