Hi Manal,
There is some old information regarding Thalassemia mutations that I came across on the internet sometime back when I was trying to find out about the mutations that my daughter has (she is double/compound heterozygous beta thalassemia major - double heteozygous (or compound heterozygous) means that both the alleles have mutations).
This material is from the book A Syllabus of Thalassemia Mutations (1997) by Titus H.J. Huisman, Marianne F.H. Carver, and Erol Baysal, published by The Sickle Cell Anemia Foundation in Augusta, GA, USA. The material is available under:
http://globin.cse.psu.edu/html/huisman/thals/contents.htmlThe specific information about the two mutations that you talked about are in the following websites (from the same material):
IVS I-6:
http://globin.cse.psu.edu/html/huisman/thals/beta/IVS-I-6.(T-@C)..the.Portuguese.type.htmlCodon 27 ( HB Knossos ):
http://globin.cse.psu.edu/html/huisman/thals/beta/Codon.27.(G-@T)..GCC(Ala)-@TCC(Ser).htmlHope this answers your question. I am not a doctor, so will not be able to explain the information in greater detail
Hi Christine,
The fetal hemoglobin decays in infants are different rates, for some it decays faster than others. In the case on my daughter it went down from mid 10s to high 8s in a week. She lost some more hemoglobin over the next two weeks and needed a transfusion when her hemoglobin level was in the low 7.
I am not sure whether the rate of decay was slightly higher than normal (the doctor had indicated that in thal majors the hemoglobin decays at the rate of 1 per week) because of the blood that was drawn out of her. But now after three transfusions, her pre-transfusion hemoglobin levels are maintained at ~ high 9 and she is most probably settling down to a once a month blood transfusion schedule.
So, if Lauryn is maintaining a hign hemoglobin, and your doctor is comfortable with not doing the DNA sequencing, I think you and Lauryn should be OK, as long as Lauryn gets the required care for thalassemia from him/her.
Remember that the DNA sequencing will only tell you exactly what Lauryn has and what the mutations of the two alleles are - it will not change the type of care that she is currentkly receiving. I think they require around 5cc of blood to do the sequencing, but your doctor may be able to tell you better.
Regards,
Bostonian