Test Name	NME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic DNA Test
Test type	ENT Doctor
Pre-test Information	Clinical History of Patient who is going for CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER19
Report Delivery	3 to 4 Weeks
Components
Price	₹ 20000
Method	NGS Technology

Short Description

NGS genetic DNA test detecets for variant and mutation detection in NME8 gene for Primary ciliary dyskinesia type 6

PreTest Information

Clinical History of Patient who is going for CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER19

Detail Description

NME8 Gene and Primary Ciliary Dyskinesia Type 6: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Introduction

Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the motility of cilia in the respiratory tract, sinuses, and ears. PCD is caused by mutations in genes that are essential for cilia structure and function. One of these genes is the NME8 gene, which is responsible for PCD type 6. In this blog, we will discuss the symptoms, diagnosis, and NGS genetic DNA test cost for PCD type 6 caused by the NME8 gene.

Symptoms of PCD Type 6

PCD type 6 caused by the NME8 gene mutation is characterized by respiratory symptoms such as chronic cough, recurrent sinus infections, and bronchiectasis. Patients may also experience hearing loss, dizziness, and infertility due to the dysfunction of cilia in the reproductive organs. Children with PCD type 6 may also have situs inversus, a condition where the internal organs are reversed from their normal position.

Diagnosis of PCD Type 6

Diagnosis of PCD type 6 involves a combination of clinical evaluation, imaging tests, and genetic testing. Clinical evaluation includes a thorough medical history and physical examination, as well as tests to assess lung function and ciliary motility. Imaging tests such as CT scan and MRI can help identify structural abnormalities in the respiratory tract. Genetic testing, including NGS genetic DNA testing, can confirm the presence of mutations in the NME8 gene.

NGS Genetic DNA Test Cost for PCD Type 6

NGS genetic DNA testing is a powerful tool for diagnosing genetic disorders such as PCD type 6 caused by the NME8 gene mutation. This test uses advanced sequencing technology to analyze multiple genes simultaneously, allowing for a comprehensive evaluation of the patient's genetic makeup. The cost of NGS genetic DNA testing for PCD type 6 in India is approximately INR 20,000.

Conclusion

PCD type 6 caused by the NME8 gene mutation is a rare genetic disorder that affects the respiratory tract, sinuses, and ears. Symptoms include chronic cough, recurrent sinus infections, and bronchiectasis, as well as hearing loss, dizziness, and infertility. Diagnosis involves clinical evaluation, imaging tests, and genetic testing, including NGS genetic DNA testing. The cost of NGS genetic DNA testing for PCD type 6 in India is approximately INR 20,000. Early diagnosis and management of PCD type 6 can help improve patient outcomes and quality of life.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for NME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic DNA Test