Short Description

NGS genetic DNA test detecets for variant and mutation detection in ARMC4 gene for Primary ciliary dyskinesia type 23

PreTest Information

Clinical History of Patient who is going for IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic DNA Test gene IARS18

Detail Description

ARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic DNA Test cost INR:20000 symptoms diagnosis - DNA Labs India

Primary ciliary dyskinesia (PCD) is a rare genetic disorder that affects the movement of cilia in the respiratory tract, causing recurrent infections, chronic cough, and breathing difficulties. The ARMC4 gene is one of the genes that can cause PCD, specifically PCD type 23. If you suspect that you or a loved one may have PCD type 23, it's important to get tested.

ARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic DNA Test cost INR:20000

DNA Labs India offers an advanced genetic test that can detect mutations in the ARMC4 gene, as well as other genes associated with PCD. The test uses next-generation sequencing (NGS) technology to analyze your DNA and provide accurate results. The cost of the test is INR 20000.

Symptoms of ARMC4 Gene Primary ciliary dyskinesia type 23

• Chronic cough
• Recurrent respiratory infections, such as pneumonia and bronchitis
• Difficulty breathing
• Ear infections
• Sinus infections
• Fertility problems

Diagnosis of ARMC4 Gene Primary ciliary dyskinesia type 23

The diagnosis of PCD type 23 involves several tests, including:

• Genetic testing to detect mutations in the ARMC4 gene
• High-speed video microscopy to analyze the movement of cilia in the respiratory tract
• Lung function tests to measure how well your lungs are working
• Chest X-ray or CT scan to look for abnormalities in the lungs

If you're experiencing symptoms of PCD type 23, it's important to see a doctor who specializes in respiratory disorders. They can refer you to a genetic testing facility like DNA Labs India for testing.

Don't wait to get tested for ARMC4 Gene Primary ciliary dyskinesia type 23. Early diagnosis and treatment can help manage symptoms and improve quality of life. Contact DNA Labs India today to schedule your genetic test.

Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the function of cilia, which are hair-like structures on the surface of cells that play a crucial role in moving mucus and fluids within the respiratory tract and other organs. Mutations in various genes, including ARMC4, have been associated with different subtypes of Primary Ciliary Dyskinesia. Here's more information about the ARMC4 gene and its link to Primary Ciliary Dyskinesia Type 23: