I tested positive for one copy of the C677T mutation
and one copy of the A1298C mutation or Methylenetetrahydrofolate reductase (
MTHFR), with hyperhomocysteinemia. Can anyone explain this in Laymens' terms?
We know have been referred to a genetic counselor, for what exactly I am not sure.
For my next round though, my ER wants to start me on Lovenox.
We are still waiting for our chromosome tests results, and should know those by Thursday...