556 top medical experts on von Hippel-Lindau Disease across 49 countries and 27 U.S. states, including 444 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- von Hippel-Lindau Disease: An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include hemangioblastoma in the retina; cerebellum; and spinal cord; pheochromocytoma; pancreatic tumors; and renal cell carcinoma (see carcinoma, renal cell). Common clinical signs include hypertension and neurological dysfunctions.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Angiomatosis (1,165), Ciliopathies (1,657), Neurocutaneous Syndromes (1,959).
- Synonyms: Familial Cerebelloretinal Angiomatosis, Lindau Disease
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