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Accurate Test Results for RSPH4A Gene Primary ciliary dyskinesia type 11 NGS Genetic DNA Test
RSPH4A Gene Primary ciliary dyskinesia type 11 NGS Genetic DNA Test Cost 20000 Rs
RSPH4A Gene Primary ciliary dyskinesia type 11 NGS Genetic DNA Test Details
RSPH4A Gene Primary Ciliary Dyskinesia Type 11 NGS Genetic DNA Test
Primary Ciliary Dyskinesia (PCD) is a genetic disorder that affects the functioning of cilia, which are tiny hair-like structures that line the respiratory tract, sinuses, and ears. PCD can cause chronic respiratory infections, hearing loss, and infertility. PCD is a rare disorder and affects approximately 1 in 15,000 people worldwide.
PCD is caused by mutations in several different genes. One of these genes is the RSPH4A gene, which is involved in the formation and function of cilia. Mutations in the RSPH4A gene can cause Primary Ciliary Dyskinesia Type 11.
NGS Genetic DNA Test is a highly advanced and accurate diagnostic tool that can detect mutations in the RSPH4A gene. The test uses next-generation sequencing technology to analyze the DNA sequence of the RSPH4A gene and identify any mutations that may be present. The test is non-invasive and requires only a small blood sample.
The cost of the RSPH4A Gene NGS Genetic DNA Test at DNA Labs India is just INR 20000. The test is performed by highly skilled and experienced professionals using state-of-the-art technology and equipment. The results of the test are available within a few days and can provide an accurate diagnosis of Primary Ciliary Dyskinesia Type 11.
Symptoms of Primary Ciliary Dyskinesia Type 11
The symptoms of Primary Ciliary Dyskinesia Type 11 can vary from person to person, but some common symptoms include:
- Chronic cough
- Recurrent respiratory infections, such as bronchitis and pneumonia
- Nasal congestion and sinus infections
- Ear infections and hearing loss
- Fertility problems
If you or someone you know is experiencing any of these symptoms, it is important to seek medical attention as soon as possible. Early diagnosis and treatment can help to prevent complications and improve quality of life.
Diagnosis of Primary Ciliary Dyskinesia Type 11
Diagnosis of Primary Ciliary Dyskinesia Type 11 can be challenging as the symptoms are similar to other respiratory conditions. The diagnosis is usually made based on a combination of clinical evaluation, medical history, and diagnostic tests.
The RSPH4A Gene NGS Genetic DNA Test is a highly accurate diagnostic tool that can detect mutations in the RSPH4A gene and provide an accurate diagnosis of Primary Ciliary Dyskinesia Type 11. The test is non-invasive and requires only a small blood sample. The test is performed by highly skilled and experienced professionals using state-of-the-art technology and equipment.
Early diagnosis of Primary Ciliary Dyskinesia Type 11 is important as it can help to prevent complications and improve quality of life. If you or someone you know is experiencing symptoms of PCD, it is important to seek medical attention as soon as possible.