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UNC119 Gene Cone-rod dystrophy NGS Genetic DNA Test Details
UNC119 Gene Cone-rod dystrophy NGS Genetic DNA Test
UNC119 Gene Cone-rod dystrophy is a rare genetic disorder that affects the retina, leading to vision loss. It is caused by mutations in the UNC119 gene. The disease is characterized by the gradual loss of cone cells, which are responsible for color vision and visual acuity, and rod cells, which are responsible for vision in low light conditions. Cone-rod dystrophy is a progressive disease, which means that vision loss worsens over time.
Symptoms of UNC119 Gene Cone-rod dystrophy
The symptoms of UNC119 Gene Cone-rod dystrophy vary depending on the severity of the disease. Some common symptoms include:
- Difficulty seeing colors
- Loss of visual acuity
- Difficulty seeing in low light conditions
- Loss of peripheral vision
- Difficulty with night vision
Diagnosis of UNC119 Gene Cone-rod dystrophy
Diagnosis of UNC119 Gene Cone-rod dystrophy is usually done by an ophthalmologist or a geneticist. The doctor will take a medical history and conduct a comprehensive eye exam. In addition, genetic testing may be recommended to identify the specific mutation causing the disease. Next-generation sequencing (NGS) genetic DNA testing is used to identify the genetic mutation that causes the disease.
NGS Genetic DNA Test for UNC119 Gene Cone-rod dystrophy
The NGS Genetic DNA Test for UNC119 Gene Cone-rod dystrophy is a type of genetic testing that uses next-generation sequencing technology to identify the specific mutation causing the disease. The test is non-invasive and involves taking a small sample of blood or saliva. The sample is then sent to a laboratory for analysis. The cost of the test is INR 20,000.
Conclusion
UNC119 Gene Cone-rod dystrophy is a rare genetic disorder that affects the retina, leading to vision loss. The disease is characterized by the gradual loss of cone cells and rod cells. Symptoms of the disease include difficulty seeing colors, loss of visual acuity, and difficulty seeing in low light conditions. Diagnosis of the disease is usually done by an ophthalmologist or a geneticist, and genetic testing may be recommended to identify the specific mutation causing the disease. NGS Genetic DNA Test for UNC119 Gene Cone-rod dystrophy is a non-invasive test that uses next-generation sequencing technology to identify the specific mutation causing the disease. The cost of the test is INR 20,000.
If you suspect that you or a loved one may have UNC119 Gene Cone-rod dystrophy, it is important to seek medical attention as soon as possible. Early diagnosis and treatment can help to slow the progression of the disease and improve the quality of life for those affected.
Contact DNA Labs India for more information on UNC119 Gene Cone-rod dystrophy and genetic testing options.
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 UNC119 Gene Cone-rod dystrophy NGS Genetic DNA Test
