Gene detection of thalassemia
The auxiliary diagnosis of thalassemia, effectively prevent severe alpha thalassemia and the birth o

Blood

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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

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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




Contact information

Address: No. 1109, Hsing three road, Ji'nan high tech Zone, Shandong

Phone: 400-966-22200

Web site: www.yinfenggene.com

Mailbox::yinfengyixuejianyan@yfyxjy.com