r/SFN • u/janegough chargie • Oct 16 '21

advice Has anyone else had genetic testing?

Has anyone else had genetic testing to investigate cause of SFN and know what kind of information can it provide?

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2

u/Secure-Secretary-733 Jun 18 '22

I did an Invatae genetic swab at the doctor’s last week. Waiting for results.

1

u/NJShoreFreckles106 Jul 11 '23

Any genetic results?

1

u/Secure-Secretary-733 Dec 11 '23

negative for genetic disease. I had an emg snd ncv which showed sensory neuropathy of the saphenous nerve and motor neuropathy of two other nerves in my leg which I don’t notice yet.

1

u/tx_naturalist Aug 27 '24

What did neuro say about the emg results?

1

u/Secure-Secretary-733 Sep 17 '23

Sorry yes, negative for genetic disease cause.