I too had all of this done and I have a 2 yr old DD....our chromomsome make-up all came back perfect but they did find something else...I have a blood clotting disorder called 'prothrombin mutation'...I had 3 m/c this year all before 6 weeks. Seems this disorder prevents blood flow to the baby.
I never would have thought they'd find something since I have a healthy 2 yr old but they did and it's genetic, it's on one set of my genes so either from mom or dad.....this means my daughter could have it too.
Doesn't make much sense to me since my pregnancy with her was perfect but after 3 heartbreaking losses, I'm glad I know - I feel guilty that it's something I had that caused my babies to die but now the next pregnancy may have a better outcome.
I say test...and test for as much as they will do
what kind of treatment do the do if they find a mistake on tehe chromosomes?
Chromosome studies on parents is Karyotyping,which is done thru blood work.Since u already have a healthy baby i don't think there should be anything worng with ur both karyotypes.But,I guess would be the docs wanna stay on the safe end.No harm is sorting things out,its after all a blood test.
I m really sorry for what u've gone thru.I Hope things better for u.
my husband and I have three and they did it on us. its just blood work and most ins cover it..