Hello I am trying to find out if going through in vitro fertilization or getting pregnant would pose any risk if you have LFS? For example, due to increased oestrogen or other medications/hormones? QS
I was told at my dx, that my family was a Li Fraumini Like family, due to the fact my sisters tumor was negative for the p53 mutation. This confuses me a little. My brother died of Ewings Sarcoma at 22 yrs old, my mother was dx 9 yrs before him at 41 yrs old
My husband tested positive for Li-Fraumini just last month. My question/concern is about my 3 adult children (ages 23, 22, 20) and whether or not they should get tested. Does anyone have anything to share about the pro’s and cons of getting tested? I have already talked to a genetics counselor and gotten their viewpoint.
Hi I’ve just met with genetics and found out my family has LFS (long suspected). I don’t yet know if I have the gene myself – my question is, if I don’t have it does that mean my daughter definitely won’t have it? (She’s 10) or can it skip to her? Thank you for any
Enrollment for a pilot study evaluating the effects of Metformin in patients with LFS is now open at The Center for Cancer Research, National Cancer Institute. Metformin is currently being studied in over sixty clinical trials of cancers including breast, colon, and uterine cancer, among others. This is the first study in patients with Li-Fraumeni
The Center for Cancer Research, National Cancer Institute, is now accepting participants for a pilot study evaluating the effects of Metformin in patients with LFS. Metformin is currently being studied in over sixty clinical trials of cancers including breast, colon, and uterine cancer, among others. This is the first study in patients with Li-Fraumeni Syndrome
