Product introduction

    PCR-Sanger sequencing was used to detect 29 kinds of gene alterations of the thalassemia gene including deletion and mutation of the alpha thalassemia related gene , and mutations of beta thalassemia releted gene. This detection can assist the clinical diagnosis of thalassemia and effectively prevent the birth of children with severe thalassemia. 

Detection process

Intended for

1. thalassemia patients - the clear cause of the disease

2. pre-pregnancy couples - assessing the risk of the birth of children with thalassemia

3. pregnant couples - preventing the birth of patients with thalassemia 

4. high risk population - childhood anemia, family history, high incidence region (Hainan, Guangxi, Yunnan, Guangdong, and Guizhou)

5. neonatal screening - early diagnosis and treatment

Technical advantage

Noninvasive - only to extract 3mL EDTA blood or newborn heel blood spots

Full coverage -- complete alpha thalassemia gene deletion and mutation, 29 mutation detection of beta thalassemia gene

The gold standard gold standard, the diagnosis of thalassemia