Just got a call from our pediatrician. Little man's heel prick test came back abnormal and we are seeing a genetic specialist Next Week for possible CUD. Anyone have this before? Could be a false positive
While I do not have any previous experience, we did just receive a call from the pediatrician that our newborn blood screening came back inconclusive. They required that we go back to the hospital and have the bloodwork done again as opposed to using those results though.
The weird part is when we asked the hospital how long the results would take they said three weeks, but we only just had our son on Friday and they appear to have results. I'm hoping it's just sensitive lab work that they double check – I hope it is the same for you. Good luck!
They geneticist said they will collect a blood and urine sample (don't know how they are going to do that) and that results will come back in a week. The pediatrician said we need to get retested asap but the specialist said we can wait for the next available appointment since the enzyme that came back low wasn't life threatening. If he does have this disorder he will like have to be on a replacement enzyme and have a restricted diet his entire life. Not the worst thing but I hope it was a false positive
So upon a discussion with our doctor today we got clarification that DS tested "borderline abnormal immune deficiency". We went for the retest and are awaiting the results.
So we are still waiting for test results, but after talking to the doctors we feel better. They basically said that his Carnatine levels could have been low because mine are naturally low. If he does have a form of this disease he will just have to take a carnatine supplement the rest of his life. Otherwise he will be normal. They will basically measure his levels in his blood and urine and compare them. If they are about the same. He is good. If they do t rest match then we need some help. So it's not as bad as the internet make it seem
So we finally got results. His urine and blood levels are still low. This doesn't mean he has the disease yet. He will take the Carnatine supplement for a week then we go back for more blood and urine. They will also run a DNA test to confirm the disorder. Kinda wish they did that the first time. So we really have two more weeks to wait this out. It's frustrating. Just want to know if my little man is OK or not.
So I finally got test results back. According to the DNA tests little man does not have the deficiency but he is a carrier. His levels got up to normal levels with the supplement. We now went back to have his levels rechecked after stopping the supplement. I also am having my levels checked to see if mine are low as well. There may be a maternal factor to it or I might have the deficiency. So long story short is that we still need to figure out why his levels are low...
Re: Carnitine uptake deficiency
The weird part is when we asked the hospital how long the results would take they said three weeks, but we only just had our son on Friday and they appear to have results. I'm hoping it's just sensitive lab work that they double check – I hope it is the same for you. Good luck!
Welcomed baby girl: 06.10.14
Second pregnancy EDD: 06.16.16 MC: 10.29.15
Welcomed baby boy: 11.25.16
Welcomed baby girl: 06.10.14
Second pregnancy EDD: 06.16.16 MC: 10.29.15
Welcomed baby boy: 11.25.16
Im sorry, I'm sure this is so stressful! I'll be keeping you guys in my thoughts and prayers!
Welcomed baby girl: 06.10.14
Second pregnancy EDD: 06.16.16 MC: 10.29.15
Welcomed baby boy: 11.25.16
We just got the call this morning and he is completely clear!
Welcomed baby girl: 06.10.14
Second pregnancy EDD: 06.16.16 MC: 10.29.15
Welcomed baby boy: 11.25.16
Welcomed baby girl: 06.10.14
Second pregnancy EDD: 06.16.16 MC: 10.29.15
Welcomed baby boy: 11.25.16