Hippel lindau syndrome
An inherited familial cancer syndrome which is characterized by development of capillary hemangioblastomas of the central nervous system and retina; clear cell renal carcinoma; pheochromocytoma; pancreatic tumors; and inner ear tumors. The syndrome is associated with germline mutations of the VHL tumor suppressor gene, located on chromosome 3p25-26. Symptoms of VHL syndrome may not be apparent until the third decade of life. CNS hemangioblastoma is the most common cause of death, followed by clear cell renal cell carcinoma. --2004
Disease Alternative Name
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
Krishna Institute Of Medical Sciences
Internship
Krishna Institute of Medical Sciences Karad.
MBBS
Maulana Azad Medical College
MBBS
Indraprastha Apollo Hospitals, New Delhi
Research Fellow
Government Medical College, Miraj
MBBS
Dr. D. Y. Patil Medical College
DNB GENERAL SURGERY
Amritsar Eye Hospital
Director
G M C Amritsar
M S ophthalmology
Esic Andheri
Senior Resident - General Surgery
Fortis Hospital Noida
DNB Neurosurgery
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