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can neurofibromatosis type 1 be detected before its symptoms appear? if so, how and when?

and

if there any way to detect a carrier of neurofibromatosis type 1?

thanks! :)

2007-05-18 09:26:13 · 2 answers · asked by coralflower 3 in Health Diseases & Conditions Cancer

2 answers

You should be able to contact the genetic department of your hospital and ask to have genetic testing done. Most hospitals will have a few questions, but if you are insured, you should get the tests you want. Ask about testing for neurofibromatosis, and if they don't have the tests available, they should be able to direct you to someplace that will.

2007-05-18 09:45:31 · answer #1 · answered by jakers 2 · 0 0

Yes, you can have genetic testing to determine if you have it.

2007-05-18 13:00:35 · answer #2 · answered by happydawg 6 · 0 0

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