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PITPNM3 Gene Cone-Rod Dystrophy Type 5 Genetic Test

Original price was: $700.Current price is: $500.

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The PITPNM3 Gene Cone-Rod Dystrophy Type 5 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the PITPNM3 gene associated with cone-rod dystrophy type 5. This inherited retinal disorder affects both cone and rod photoreceptor cells, leading to progressive vision loss, color vision impairment, and photophobia. Using next-generation sequencing technology, this comprehensive test provides accurate detection of genetic variants responsible for this condition. Early identification through genetic testing enables proactive management strategies and helps guide treatment decisions. The test costs $500 USD and is particularly valuable for individuals with family history of retinal disorders or those experiencing early symptoms of vision deterioration. Results are typically available within 3-4 weeks, providing crucial information for patients and their healthcare providers.

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PITPNM3 Gene Cone-Rod Dystrophy Type 5 NGS Genetic DNA Test

Comprehensive Genetic Testing for Inherited Retinal Disorders

The PITPNM3 Gene Cone-Rod Dystrophy Type 5 NGS Genetic DNA Test represents a breakthrough in ophthalmic genetic diagnostics, offering precise detection of mutations associated with this specific form of inherited retinal dystrophy. Cone-rod dystrophy type 5 is a progressive eye condition that primarily affects the retina’s photoreceptor cells, leading to significant visual impairment over time. This advanced genetic test utilizes next-generation sequencing technology to provide comprehensive analysis of the PITPNM3 gene, enabling early diagnosis and personalized management strategies for affected individuals and their families.

What Does This Test Measure and Detect?

This specialized genetic test focuses on identifying mutations within the PITPNM3 gene, which plays a crucial role in retinal function and photoreceptor cell maintenance. The test specifically detects:

  • Pathogenic variants in the PITPNM3 gene associated with cone-rod dystrophy type 5
  • Single nucleotide polymorphisms (SNPs) affecting retinal development
  • Deletions, insertions, and other structural variations in the gene sequence
  • Autosomal dominant inheritance patterns characteristic of this condition
  • Genetic markers that indicate disease progression risk

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals experiencing symptoms or having risk factors for cone-rod dystrophy type 5, including:

  • Patients with progressive vision loss beginning in childhood or early adulthood
  • Individuals experiencing difficulty with color vision and contrast sensitivity
  • Those with photophobia (light sensitivity) and night blindness
  • Patients showing characteristic retinal changes on ophthalmological examination
  • Individuals with family history of inherited retinal disorders
  • People seeking genetic counseling for family planning purposes
  • Patients with unexplained visual field defects or central vision loss

Key Benefits of PITPNM3 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:

  • Early Diagnosis: Enables detection before significant vision loss occurs
  • Personalized Management: Guides tailored treatment and monitoring strategies
  • Family Planning: Provides crucial information for genetic counseling
  • Proactive Intervention: Allows for early implementation of vision preservation techniques
  • Accurate Prognosis: Helps predict disease progression and visual outcomes
  • Research Contribution: Advances understanding of retinal genetic disorders

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of genetic specialists and ophthalmologists. Positive results indicating PITPNM3 gene mutations confirm the diagnosis of cone-rod dystrophy type 5 and provide valuable information about inheritance patterns. Negative results may help rule out this specific genetic cause, though additional testing might be recommended for comprehensive evaluation. All results include detailed explanations and recommendations for next steps, including potential treatment options, lifestyle modifications, and ongoing monitoring requirements.

Test Details and Pricing

Test Component Details
Test Name PITPNM3 Gene Cone-Rod Dystrophy Type 5 NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Pre-Test Requirements and Preparation

To ensure accurate results and comprehensive care, we recommend:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create detailed family pedigree chart
  • Discussion of potential implications and outcomes with healthcare provider
  • Review of insurance coverage and payment options

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many more. Our network of certified genetic testing facilities ensures consistent quality and reliable results regardless of your location.

Take Control of Your Eye Health Today

Don’t wait to get the answers you need about your vision health. Early genetic testing for cone-rod dystrophy type 5 can provide critical information for managing your condition and preserving your vision. Our team of genetic specialists and ophthalmologists are ready to guide you through the testing process and help you understand your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your PITPNM3 genetic test and take the first step toward comprehensive eye health management.