KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test - $500 USA Price | Comprehensive Genetic Testing
Sale!

KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test

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

-29%

The KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the KLHL3 gene responsible for Pseudohypoaldosteronism Type 2D, a rare inherited vascular disorder affecting blood pressure regulation. Using Next-Generation Sequencing (NGS) technology, this comprehensive test provides precise detection of genetic variants that disrupt normal aldosterone signaling pathways. The test is essential for individuals experiencing unexplained hypertension, electrolyte imbalances, or with family histories of similar conditions. Results help guide personalized treatment strategies and provide crucial information for family planning. Available for $500 USD, this test offers significant savings from the regular $700 price, making advanced genetic testing accessible to patients across the United States.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Vascular Disorders

The KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for rare inherited vascular conditions. This advanced genetic test specifically targets mutations in the KLHL3 (Kelch-like protein 3) gene, which plays a critical role in regulating blood pressure and electrolyte balance through the aldosterone signaling pathway.

What This Test Measures and Detects

Using state-of-the-art Next-Generation Sequencing (NGS) technology, this comprehensive genetic analysis identifies:

  • Pathogenic variants in the KLHL3 gene associated with Pseudohypoaldosteronism Type 2D
  • Single nucleotide polymorphisms (SNPs) affecting protein function
  • Insertions, deletions, and missense mutations disrupting normal gene expression
  • Genetic markers linked to impaired renal sodium handling and potassium regulation
  • Inheritance patterns for family risk assessment

Who Should Consider This Genetic Test

This specialized genetic test is recommended for individuals experiencing:

  • Early-onset hypertension resistant to conventional treatments
  • Unexplained electrolyte imbalances, particularly hyperkalemia
  • Family history of Pseudohypoaldosteronism Type 2D or similar disorders
  • Metabolic alkalosis with normal renal function
  • Hypertension accompanied by suppressed plasma renin activity
  • Children or young adults with severe hypertension
  • Individuals with suspected familial hyperkalemic hypertension

Significant Benefits of Genetic Testing

Undergoing the KLHL3 Gene Pseudohypoaldosteronism Type 2D test provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out genetic causes of hypertension
  • Personalized Treatment: Guides targeted therapeutic approaches
  • Family Planning: Provides crucial information for genetic counseling
  • Early Intervention: Enables proactive management of potential complications
  • Peace of Mind: Reduces uncertainty about inherited conditions
  • Comprehensive Care: Supports integrated treatment planning with healthcare providers

Understanding Your Test Results

Your genetic test results will be thoroughly explained by our certified genetic counselors:

  • Positive Result: Indicates the presence of KLHL3 gene mutations associated with Pseudohypoaldosteronism Type 2D, requiring specialized medical management
  • Negative Result: Suggests that KLHL3 gene mutations are not the cause of your symptoms, directing further diagnostic evaluation
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical implications, requiring ongoing monitoring
  • Carrier Status: Determines if you carry the gene mutation without showing symptoms, important for family planning

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Nationwide Testing Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection centers ensures accessible genetic testing for patients nationwide.

Pre-Test Requirements and Genetic Counseling

Before undergoing testing, patients should provide:

  • Complete clinical history relevant to Pseudohypoaldosteronism Type 2D symptoms
  • Participation in a genetic counseling session to create a detailed family pedigree
  • Documentation of affected family members and their medical histories
  • Current medication list and previous diagnostic test results

Ready to take control of your genetic health? Book your KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test today by calling our dedicated genetic testing specialists at +1(267) 388-9828 or schedule your appointment online. Our team is available to answer your questions and guide you through the testing process with compassion and expertise.

SKU: 64a7157cf393 Category: