Has anyone here used Peyronie's Gene Test Kit from pathright medical? Was it accurate? What was the cost?

I had no idea about this! Very interesting. Haven't used it, but made a search on, their website and was very impressed that Dr Landon and his colleagues came up with it.

I'll leave the website for people wondering about it:
www.pathrightmedical.com/product/peyronies-gene-test/

This is pretty interesting. As with many kits like this, just because you have the gene doesn't mean you will contract Peyronies. If I knew I had the gene, I would definitely be careful to avoid any type of penile injury.
It will be interesting to see any feedback on this. Since I've had Peyronies, would be interesting to see if I tested positive for the gene.

I wonder if there are people who test negative for the gene and have symptoms that resemble peyronies disease.

Bentknob:

possible. I fracture my penis in 2014. Got curvature, slight length loss and ED as a result. First ultrasound i did also showed fibrous tissue. But i don't have Peyronies. Just the results of the fracture itself.

Pfract:

I believe my case resembles peyronies disease but may not be actual peyronies.

A urologist said mine sounds like an injury. I'm not surprised due to my lifestyle.

I was taking double the recommended dose in erectile dysfunction medications and combining them so I could hold an erection for hours and have vigorous sex with multiple women a night at sex parties.