Experiences with

Genetic test

Dear all , I just got genetic report of my father which is showing a variant TP53 p.lle195Phe . Are there any specific agents to target this mutation ? He is currently paralyzed below waist and is on chemo cabazitaxel 35 mg , completed 5 infusion till date . Below is his PSA summary after starting

My doctor decided to test me for this. I did a genetic test says I have the mutations for this and now she want to send me for this nose noxide test. I was wondering if if anyone else got tested for this before and wondering how accurate the genetic test is. I appreciate any responses

My son has recently been diagnosed with DCM and I came across some info suggesting first degree relatives should be referred to a specialist clinic to be checked out. The BHF apparently will provide a letter to your GP to support this referral. How does this work. Will there be a fee for the letter?

The notation "++COMT V158M" in a genetic test report generally refers to the presence of the Val158Met polymorphism in the COMT gene, with specific implications as follows: 1.

Since then, researchers have been developing a genetic test for the condition, which they plan to make available in the UK.

in February I shall be seeing the neurologist who made the initial diagnosis to see if I do have CANVAS by a genetic test. But I was wondering if anybody here has it?

I thought all germline genetic test were the same. I am also having his biopsy slides sent over to his new oncologist for second opinion. We never received any documentation on his somatic testing claiming this mutation. We were only told this by his urologist after biopsy.

Just after chemotherapy I had a genetic test which came back positive for the BRCA2 mutation. I wonder if anyone out there has the mutation and if it resulted / correlated in multiple cancers? The kidney mass has basically grown/changed very little since day one.

Since my C-peptide level is still quite high and I have no antibodies, a genetic test for MODY was done. It turns out I have MODY Type 10 (INS), which seems to be a very rare form of MODY. Is anyone else here with Type 10?

test 6 - Vitamin D for the bones (from dr Saad) and Bone Protective Agents are great also to prolong OS, especially with Radium 7 - Clinical trials are becoming more widespread and secure 8 - Thanks Prostate Cancer Foundation for helping research That's basically it (I intentionally did not pay

My CF test result was 58 so I did the genetic test to confirm whether I have CF or otherwise and that came back negative thankfully.

Genetic test: negative, MSI High Three MOs reviewed my case, and they concluded that although I have a high Gleason score, based on CHAARTED and LATTITUDE, I have a low-volume, low-risk disease (no visceral involvement, 1 site of bony disease).

He told me that the hospital still had my tumor and he requested a genetic test on the sample. Sure enough, I tested positive for VHL. I am one of the lucky ones that accidentally for the kidney tumors during a CT scan for something unrelated.

One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I was originally told it was not genetic.

I am adding some nutritional supplements - and want the genetic test to let me know about the MTHFR gene as well. I feel so overwhelmed trying to navigate all of this. Those of you who have found a good combination of meds and are seeing progress for your kids have given me hope to keep trying.

This info plus a comprehensive new Gardian DNA blood genetic test showed us some new options based on my mutations/bio markers (I am an architect so firgive me if I get this wrong) posting in case anyone needs info for themselves later: ESR1 suggest: Elacestrant (option) and Letrozole(already had)

I am concerned about the new genetic test AvertD just approved by the FDA https://www.washingtonpost.com/health/2024/03/25/dna-test-opioid-addiction/ It uses DNA to predict whether a person is likely to get addicted to opioids.

I found out as hubby bought me a Family history genetic test as a present and it included health DNA results.

I was recently diagnosed with hemochromatosis based on slightly off bloodwork and genetic test. Neither of my parents had hemochromatosis but both were carriers and I inherited the gene from both.

test t o see what kind of medications i can take, which im not keen on because i started lexapro when i was younger and couldnt metabolize it and it made my anxiety 10x worse. and the genetic test revealed that i have the anxiety and depression gene, like the genetic that is connected to anxiety. it