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Thread: F508 & d110h

  1. #21
    Super Moderator
    Join Date
    Mar 2012
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    2,035
    Cd odd?..how was he diagnosed? did they do a sweat test? Level?

  2. #22
    Junior Member
    Join Date
    May 2015
    Posts
    5
    My son was diagnosed through the newborn screening. His sweat test was 43/58. He had "borderline" results after two sweat tests. My daughter's sweat test was in the 70's/80's. We were actually told that she was a carrier when she was 6 wks. after her newborn screening showed the F508 mutation. Not sure when the d110h mutation was discovered but she was born 1/31/10. She was considered a "missed diagnosis" after her newborn labs were sent back for review in 2014 and came back showing both F508/d110h.

  3. #23
    Jeannie85
    Guest
    I am pretty much on the same boat as you as far as my daughter having ZERO symptoms. And she is healthier than most of our friends children. It's frustrating but I also pray it stays like that for as long as possible. She is PS also, no vitamins or supplements. She was started on albuterol immediately after diagnosis but also never has had a breathing problem. We did CPT til she was a year and now do the vest. Also after she cultured staphylococcus x3 clinic appointments, they started pulmozyme. I am pregnant with our second baby and im anxious to find out if he or she will have cf also.

  4. #24
    Junior Member
    Join Date
    May 2015
    Posts
    5
    First of all, congratulations on your pregnancy! I'll be praying for you and your baby. Second, I'm soooo glad to hear of another symptom free child with the same mutations. PS, I also have an 11 yr old who does not have CF.

  5. #25
    Jeannie85
    Guest
    Thank you!

  6. #26
    Junior Member
    Join Date
    Nov 2018
    Posts
    5
    good day we are from Slovakia and we have son of cf mutation D110H and deletion of xenon 4-6 ake mate or prognosis for this mutation son 1 year without signs cf in addition to sweat 60 moles in reply thank you

  7. #27
    Junior Member
    Join Date
    Nov 2018
    Posts
    5
    good day our son has skrining on cf mutation D110H and deletion xenon 4-6 also does not have any symptoms 1 year ago how do you handle the ake mate experience? we welcome the healing of the Slovak republic

  8. #28
    Junior Member
    Join Date
    Sep 2016
    Posts
    13
    I do not understand what you are asking. Could you try to rephrase it?

  9. #29
    Junior Member
    Join Date
    Nov 2018
    Posts
    5
    Hello. I'm from Slovakia. I have a son, 1 year old. Has mutations D110H and deletion exons 4,5 and 6. Is there anyone who has this mutation D110H ??? How are you doing? What are the symptoms? Well thank you. I greet all.

  10. #30
    Junior Member
    Join Date
    Sep 2016
    Posts
    13
    My 5 year old daughter has d110h and delta508. She has been healthy other than kid stuff like colds due to being in school. Last year she had recurring ear infections but then got tubes placed and has had no ear infections since. She is on Kalydeco and has been for a little over a year. She has no digestive issues. We did get a sweat test done a short time ago, for a research study. At 2 weeks old her results were 71 and 67. With Kalydeco the results were 24 and 25!!!

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