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Thalassemia is an inherited blood disorder characterised by less oxygen-carrying protein (haemoglobin) and fewer red blood cells in the body than normal.
Symptoms include fatigue, weakness, paleness and slow growth.
Mild forms may not need treatment. Severe forms may require blood transfusions or a donor stem-cell transplant.
थैलेसीमिया एक विरासत में मिला रक्त विकार है जिसकी विशेषता कम ऑक्सीजन-युक्त प्रोटीन (हीमोग्लोबिन) और शरीर में कम लाल रक्त कोशिकाएं हैं।
लक्षणों में थकान, कमजोरी, paleness और धीमी वृद्धि शामिल है।
हल्के रूपों को उपचार की आवश्यकता नहीं हो सकती है। गंभीर रूपों में रक्त आधान या दाता स्टेम सेल प्रत्यारोपण की आवश्यकता हो सकती है।
Thalassemia is an inherited blood disorder characterised by less oxygen-carrying protein (haemoglobin) and fewer red blood cells in the body than normal.
Symptoms include fatigue, weakness, paleness and slow growth.
Mild forms may not need treatment. Severe forms may require blood transfusions or a donor stem-cell transplant.