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Cystic fibrosis (R117H)? |
I AM 25 WEEKS PREGNANT AND JUST FOUND OUT IM A CARRIER FOR CYSTIC FIBROSIS. MY HUSBAND HAS BEEN TESTED BUT WE ARE AWAITING THE RESULTS. HE IS AFRICAN AMERICAN/ HINDU SO IM TOLD THE CHANCE IS LOWER? MY QUESTION IS( THERE TELLING ME THIS IS A RARE FORM THEY NEVER HEARD OF .(R117H) IM CURIOUS TO KNOW WHAT THIS MEANS IF THIS IS WORSE BETTER THE SAME OF THE DELTA FORM?IF ITS LIKELY TO PASS ON TO MY UNBORN SON? THIS IS ALL NEW TO ME, NO ONE IN MY FAMILY HISTORY HAS HAD BEEN AWARE OF THIS AND NOW IM IN THATLOW PERCENTILE OF BEING A CARRIER? PLEASE ANYHELP OR INFO ON THIS WOULD HELP SOO MUCH? Actually, the R117H mutation was discovered several years ago. The fact that you carry the mutation does not mean your child will have cystic fibrosis. Your husband must also have the genetic defect. If you are both carriers, your child will have a one in four chance of having cystic fibrosis. Here's how it works: Calm down, don't worry. I am a carrier. My daughter had to have a sweat test when she was born - and she is a carrier too. My son is not. It's a new test. I will just warn her when she gets older to be sure her husband is not so they don't pass it on - you need to have two carriers to have a baby active with CF. |
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