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SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test

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

-29%

The SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test is a cutting-edge genetic screening method that identifies mutations in the SEMA3A gene associated with Kallmann syndrome. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that disrupt normal hormonal development and function. Kallmann syndrome is a rare genetic condition characterized by delayed or absent puberty and an impaired sense of smell, affecting both reproductive health and neurological development. The test provides crucial diagnostic information for individuals experiencing delayed puberty, infertility, or olfactory dysfunction. By identifying the specific SEMA3A gene mutation, healthcare providers can develop targeted treatment strategies and provide accurate genetic counseling. This test is particularly valuable for patients with family histories of hormonal disorders or unexplained reproductive health issues. The comprehensive analysis includes detailed reporting of genetic variants and their clinical significance. Available for $500 USD, this advanced genetic test offers significant insights into complex endocrine and reproductive conditions.

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SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for Hormonal and Reproductive Health

The SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for complex endocrine disorders. This advanced testing methodology provides crucial insights into the genetic basis of Kallmann syndrome, a rare condition affecting both reproductive development and olfactory function. Our state-of-the-art laboratory utilizes cutting-edge Next-Generation Sequencing technology to deliver accurate, reliable results that empower patients and healthcare providers with essential diagnostic information.

What Does the SEMA3A Gene Kallmann Syndrome Test Measure?

This comprehensive genetic analysis specifically targets the SEMA3A gene, which plays a critical role in neuronal migration and the development of the hypothalamic-pituitary-gonadal axis. The test identifies:

  • Pathogenic variants in the SEMA3A gene associated with Kallmann syndrome
  • Single nucleotide polymorphisms (SNPs) affecting gene function
  • Copy number variations and structural abnormalities
  • Novel mutations with potential clinical significance
  • Genetic markers influencing treatment response and prognosis

Who Should Consider This Genetic Test?

This specialized genetic testing is recommended for individuals presenting with:

  • Delayed or absent puberty beyond expected developmental timelines
  • Complete or partial anosmia (loss of smell)
  • Unexplained infertility or reproductive challenges
  • Family history of Kallmann syndrome or related endocrine disorders
  • Congenital hypogonadotropic hypogonadism symptoms
  • Associated neurological or developmental concerns
  • Multiple family members with hormonal or reproductive issues

Significant Benefits of SEMA3A Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out Kallmann syndrome with high precision
  • Personalized Treatment: Enables targeted hormonal therapy based on genetic findings
  • Family Planning: Provides essential information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates timely management of associated health concerns
  • Comprehensive Understanding: Offers insights into the underlying biological mechanisms
  • Peace of Mind: Reduces uncertainty and provides clear diagnostic direction

Understanding Your Test Results

Our comprehensive genetic report provides detailed interpretation of your results:

  • Positive Result: Indicates the presence of pathogenic SEMA3A gene variants associated with Kallmann syndrome. This confirms the genetic diagnosis and guides appropriate medical management.
  • Negative Result: Suggests that SEMA3A gene mutations were not detected, though other genetic or non-genetic causes should still be considered.
  • Variant of Uncertain Significance: Some genetic changes may require additional clinical correlation and family studies for proper interpretation.
  • Carrier Status: Identifies individuals who may carry the genetic variant without showing symptoms.

All results are accompanied by detailed clinical interpretation and recommendations from our expert genetic counseling team.

Test Pricing and Availability

Test Component Price (USD)
SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test – Discount Price $500
SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test – Regular Price $700

Nationwide Testing Availability

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

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about your hormonal health or reproductive concerns continue. Our specialized genetic testing provides the answers you need for informed medical decisions and personalized treatment approaches. With rapid turnaround times of 3-4 weeks and comprehensive genetic counseling support, we’re committed to delivering exceptional care and accurate results.

Book your SEMA3A Gene Kallmann Syndrome NGS Genetic DNA Test today by calling our dedicated genetic counseling team at +1(267) 388-9828 or schedule your appointment online. Take control of your genetic health journey with confidence and clarity.