Hi to everyone. First of all, congratulation for creating this page. I have read thru the page and everyone is so wonderful and supportive. Please excuse my English. I am from Malaysia, suspected thal minor (cant be sure if its a or b), no confirmation test carried out. But due to my high RBC, normal HB with persistenly low MCV and MCH, doctor suggested that I might have thal minor. My daughter is now almost 10 months old. My wife is currently pregnant with our 2nd baby (13 weeks) and still waiting for her thalassemia test result (her cbc indicates anemia with low hb,mcv and mch). Unfortunately, no thal test was carried out during her pregnancy with our first daughter, MyAmaanat (Gods gift to me) Lil Nuha. So far Nuha is a bit slow in development (weight and height are in the 3rd-10th percentile). Other than that, she is quite active, feeding well. I didnt notice any significant paleness, jaundice or severe fatigue in her. I am worried that she might inherit something serious. My questions are:
1-When do normally symptoms of b-thal major start to appear in infants/babies?
2-When do normally symptoms of b-thal intermedia start to appear in infants/babies?
3-If there are no symptoms, by what age can I safely ruled out thal major/intermedia?
Any feed backs on my question is greatly appreciated. My pray goes out for everyone here.
Best Regards.
MAN