Why do you need to carry out genetic testing f&☆∏or thalassaemia?

  Thalassemia (abbreviated as thalassemΩ∞Ω ia), also known as globin prod'©uction disorder anemia, is a group of inhe♥γ ‍rited hemolytic anemia diseases. Anemia ™§¥or pathological condition caused by lack or in   ¥sufficiency of synthesis of o •®☆ne or more globin chains i£∑πn hemoglobin due to inherited genetic defects ↑. According to the "Chinese Thalassae♥≥mia Blue Book (2015)", there are about 300,000 ε↑δpeople with heavy and intermediate thalas♣☆saemia in China, and↔$ the "thalassaemia" gene carrier excee&≠✔★ds 30 million, involving nearly 30 millδ¶✔βion families and 100>♠α™ million people, mainly concentrated iα$n To the south of the Yangtze River, espe©×÷cially in Guangxi and Yunnan, the most sever‌∑•✘e. Therefore, medical advice   is to conduct pre-marita•€α•l examination and prenatal geneti☆β> c diagnosis to avoid✔∑ the occurrence of the next gener$•÷ation of children.

  The thalassemia gene deσ✔÷tection kit of 100 million cubic meterσ≥×φs covers Thai type, 30M site and -50M sit​±✘e. The overall mutat​↑ion site coverage rate is±∑♠" more than 95%, which can effectively pr×✘★event missed detectiδ×γ≤on.