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Racial differences in tumor disorder.


Two people with an identical genetic defect may suffer widely different medical problems. In the case of neurofibromatosis Neurofibromatosis Definition

Neurofibromatosis (NF), or von Recklinghausen disease, is a genetic disease in which patients develop multiple soft tumors (neurofibromas). These tumors occur under the skin and throughout the nervous system.
, researchers from Washington, D.C., and Ohio have found that whites are more likely than blacks to suffer from benign, yet potentially dangerous, optic nerve tumors.

"What this tells us is that single-gene disorders manifest themselves with respect to the other genes in individual carriers," says Howard M. Saal of the Children's Hospital Medical Center in Cincinnati.

Saal and colleagues at the Children's National Medical Center This article or section is written like an .
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 in Washington, D.C., studied 372 children with neurofibromatosis, a disease marked by tumors of the skin and central nervous system and skin pigmentation known as cafe au lait spots ca·fé au lait spots
pl.n.
Uniformly light brown, sharply defined, and usually oval-shaped patches of the skin characteristic of neurofibromatosis, though also found in healthy individuals.
. Using magnetic resonance imaging magnetic resonance imaging (MRI), noninvasive diagnostic technique that uses nuclear magnetic resonance to produce cross-sectional images of organs and other internal body structures.  (MRI 1. (application) MRI - Magnetic Resonance Imaging.
2. MRI - Measurement Requirements and Interface.
), the team found optic nerve tumors, which can cause blindness and pituitary problems, in roughly 1 out of 5 white children but in only 1 out of 62 black children.

Saal says the finding illustrates how differences in other genes can affect neurofibromatosis. However, he recommends MRI scans for all children with the disease, because 7 to 10 percent suffer from malignant brain tumors regardless of race.
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Article Details
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Author:Seachrist, Lisa
Publication:Science News
Article Type:Brief Article
Date:Nov 11, 1995
Words:186
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