What Genetic Testing Should I do Before Pregnancy? - Carrier Screening.

Hi can you answer my question please
If we do genetic tests and results show me or my husband is a carrier of any mutation but we want to conceive naturally can we get any medical help other than IVF?
We have already 1 healthy child and after that 2 recurrent miscarriages.
I already checked for blood clotting disorder and I have factor V R2 mutation and PAI-1 can this be a reason for 2 failed pregnancies?

😍 Promo-SM

HFE type 1 risk in African American

Does amniocentesis confirm for sure if baby will have the disease/symptoms versus being just a carrier of the gene like the parents?

How high is the chance of the child being affected if only one parent is the carrier for a specific genetic disease?

Hi I have 2 failed IVFs, had a miscarriage with natural conception 2 years back. Got karyotype testing done, my partners tests are normal but I have ,dup(15)(q11.2q13).ish dup(15)(D15Z1+,SNRPN++,UBE3A++,PML+,15qter+) with no symptoms.
Does it mean I cannot conceive naturally and I have high chances of having a failed pregnancy or having abnormalities in baby if conceived?

I am completely clueless on the topic. But can these test help to detect certain eye diseases as well? Thank you for educating us.

Hi, I have my eggs frozen. Can my partner still get his sperm tested before we make embryos? And if we do get this testing done, should we still do the PGT-A testing for the embryos?

An ObGyn I asked seemed to think I was ridiculous to want to screen, saying it’s impossible to screen for everything under the sun… so don’t test for anything unless your parents have something obvious