Why do you need to carry out↔≈ genetic testing for thalassaemia?

  Thalassemia (abbreviated as th ✘♣alassemia), also known as globin production dis≈•order anemia, is a group of inhe≠↔∏rited hemolytic anemia ↕©₽diseases. Anemia or pathological condition÷↔∞ caused by lack or insufficiencyφ♣↓☆ of synthesis of one‍↔♥ or more globin chains in hemoglobin due t¶₹o inherited genetic defects≠©. According to the "Chines♣≥↕e Thalassaemia Blue Booπ∑k (2015)", there are about 30☆ 0,000 people with heavy and intermediate thalassa× 'emia in China, and the​₩♦  "thalassaemia" gene£≠≥ carrier exceeds 30 million, involving neλ&arly 30 million families and 10♣≠0 million people, mainly Ω∞concentrated in To the §&δsouth of the Yangtze River, especially in G±α§ uangxi and Yunnan, thφ&→e most severe. Therefore, medical adv'γ→ice is to conduct pre-marit§≠★σal examination and prenatal genetic diag♥"☆ nosis to avoid the occurrence♣Ω of the next generation oσ←f children.

  The thalassemia gene detection kit o♥δ£f 100 million cubic meters covers Th€βai type, 30M site and -50M site. The ov™☆erall mutation site coverage rate is more tha♦≤φn 95%, which can effectively prevent missed detecγβtion.