Short Description

NGS genetic DNA test detecets for variant and mutation detection in DNAI1 gene for Primary ciliary dyskinesia type 1

PreTest Information

Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN37

Detail Description

DNAI1 Gene Primary Ciliary Dyskinesia Type 1 NGS Genetic DNA Test

Primary ciliary dyskinesia (PCD) is a rare genetic disorder that affects the cilia in the respiratory tract, sinuses, and ears. It is caused by mutations in the DNAI1 gene, which encodes for a protein called dynein axonemal intermediate chain 1.

PCD type 1 is caused by mutations in the DNAI1 gene and is inherited in an autosomal recessive manner. Symptoms of PCD type 1 include:

• Chronic cough
• Recurrent infections of the respiratory tract, sinuses, and ears
• Shortness of breath
• Clubbing of fingers and toes
• Male infertility

Diagnosis of PCD type 1 can be difficult as the symptoms are similar to other respiratory conditions. However, genetic testing can confirm the presence of mutations in the DNAI1 gene. Next-generation sequencing (NGS) is a powerful tool for identifying mutations in genes and is commonly used for genetic testing.

At DNA Labs India, we offer DNAI1 Gene Primary Ciliary Dyskinesia Type 1 NGS Genetic DNA Test at a cost of INR 20,000. This test is performed using state-of-the-art equipment and technology to ensure accurate and reliable results.

If you or a loved one is experiencing symptoms of PCD type 1 or have a family history of the condition, it is important to get tested. Early diagnosis and treatment can improve outcomes and quality of life.

Contact DNA Labs India today to learn more about our DNAI1 Gene Primary Ciliary Dyskinesia Type 1 NGS Genetic DNA Test and schedule your appointment.