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Von Recklinghausen
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∙ 12y ago
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When was neurofibromatosis discovered?
Neurofibromatosis type 1 (NF1) was first described in 1882 by the German pathologist Von Recklinghausen. Neurofibromatosis type 2 (NF2) was first described in 1820 by the Scottish surgeon JH Wishart.
Who discovered neurofibromatosis?
The person credited with the discovery of neurofibromatosis is Fredich Daniel van Recklinghausen. He released an article identifying it back in 1882.
Can a prenatal test detect neurofibromatosis?
Clinical genetic testing can confirm the presence of a mutation in the neurofibromatosis type 1 (NF1) gene. Prenatal testing for NF1 mutations is also possible using amniocentesis or chorionic villus sampling procedures. Genetic testing for neurofibromatosis type 2 (NF2) mutations is sometimes available but is accurate only in about 65 percent of those individuals tested.
What is neurofibromatosis?
There are no available treatments for the disorders which underlie either type of neurofibromatosis. To some extent, the symptoms of NF-1 and NF-2 can be treated individually. Skin tumors can be surgically removed. Some brain tumors.
Which of the following is an example of an autosomal dominant disease A Huntington's disease and neurofibromatosis type 1 or B Alzheimer's Disease and Heart Disease?
Huntington's Disease
What has the author Boris Kin Lin written?
Boris Kin Lin has written: 'Characterization of the neurofibromatosis type 1 gene product and its interaction with RAS'
How did neurofibromatosis get its name?
http://en.wikipedia.org/wiki/Neurofibromatosis
What conditions cause inherited pheochromocytomas?
Multiple Endocrine Neoplasia, type 2A (MEN2A), Multiple Endocrine Neoplasia, type 2B (MEN2B), von Hippel-Lindau disease (VHL) and Neurofibromatosis type 1 (NF1).
What is the cause of neorofibromatosis?
The cause of neurofibromatosis type 1 is a genetic mutation in the NF1 gene. This gene is the one that produces a protein that helps regulate the growth of nerve tissue.
What did Francis Collins discover?
He discovered genes causing cystic fibrosis, neurofibromatosis, and Huntington Chorea. (i would spell check this answer) please look to further references.
How can neurofibromatosis be diagnosed?
Neurofibromatosis is usually diagnosed when the patient has 10 or more cafe-au-lait spots.
Are there any support groups for neurofibromatosis?
Yes, in Dallas, Texas it is called the NSG (Neurofibromatosis Support Group)
