Because NF1 is an unpredictable disorder, it varies widely in severity – even among two people in the same family. Some people with NF1 may be completely unaware that they are affected, experiencing ...
(SALT LAKE CITY)—As a postdoctoral fellow at the University of Utah's Eccles Institute of Human Genetics, David H. Viskochil, M.D., Ph.D, led the discovery of the gene that causes neurofibromatosis ...
Q: A doctor said the rashes on my son's back were “coffee spots” and that meant he might have neurofibromatosis. I read there is a new treatment for this condition; is it a cure? A: Café-au-lait spots ...
NF-1 is a genetic condition that causes brown skin patches, similar to birthmarks, and tumours 1. While the tumours are often benign, they can become cancerous over time and may cause a range of ...
Contemporary Approach to Neurofibromatosis Type 1–Associated Malignant Peripheral Nerve Sheath Tumors. If you have the appropriate software installed, you can download article citation data to the ...
Treatment for neurofibromatosis type 1 may involve surgery, radiation, chemotherapy, or other methods. In some cases, doctors may take a “wait and see” approach. Neurofibromatosis type 1 (NF1), ...
Share on Facebook. Opens in a new tab or window Share on Bluesky. Opens in a new tab or window Share on X. Opens in a new tab or window Share on LinkedIn. Opens in a new tab or window A decade of ...
DETROIT — The family foundation of Cleveland Cavaliers owner Dan Gilbert has announced a $21 million grant commitment to help accelerate the search for a cure for neurofibromatosis. Gilbert's son, ...
Neurofibromatosis type 1 (NF1) is the most common of the three types of neurofibromatosis and is also one of the most common inherited neurological disorders, affecting about 1 in 3,000 people ...
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