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Von Hippel-Lindau Syndrome

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Von Hippel-Lindau Syndrome
Pathology
Type

Genetic

Cause(s)

Faulty chromosome from mother

Symptoms

Vision problems, headaches, balance problems, dizziness, high blood pressure, weakness

Mortality Rate

Moderate if untreated

Treatments

Surgical removal of tumors

Show Information
Appearances

The Right Stuff, Mr. Fearless

  [Source]


Hippel Lindau

An MRI showing hemangioblastomas in the brain and spine of a VHLS patient, courtesy Public Library of Science, via Wikipedia

Von Hippel-Lindau Syndrome is a rare genetic disease which, like tuberous sclerosis, causes numerous small tumors (hemangioblastoma) to grow throughout the body. Although the tumors are often benign, they tend to congregate in the eyes, on blood vessels, and on glands. This causes blindness, high blood pressure, metabolic symptoms (such as sudden rage or muscle weakness).

The only treatment is surgical removal of the tumors before they become dangerously large. Patients require lifetime monitoring to ensure that no new tumors grow. The prognosis for patients is usually poor if the tumors become large, widespread, or are located in areas which are inaccessible to surgery.

Von Hippel-Lindau disease at Wikipedia

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