HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Hand-Foot-Genital Syndrome
The HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations associated with Hand-Foot-Genital Syndrome, a rare genetic disorder affecting multiple body systems. This advanced genetic analysis provides crucial insights for patients and families dealing with unexplained developmental abnormalities.
What Does This Test Measure?
This specialized genetic test utilizes Next Generation Sequencing (NGS) technology to comprehensively analyze the HOXA13 gene for pathogenic variants. The test specifically detects:
- Point mutations in the HOXA13 gene coding regions
- Small insertions and deletions affecting gene function
- Genetic variations disrupting normal protein production
- Inherited and de novo mutations causing developmental abnormalities
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with symptoms suggestive of Hand-Foot-Genital Syndrome, including:
- Newborns or children with hand malformations (short thumbs, clinodactyly)
- Individuals with foot abnormalities (short great toes, syndactyly)
- Patients with genitourinary anomalies (hypospadias, uterine abnormalities)
- Those with family history of limb or urogenital malformations
- Individuals with unexplained developmental delays affecting extremities
Clinical Benefits of Genetic Testing
Undergoing the HOXA13 Gene Guttmacher Syndrome test offers numerous advantages:
- Accurate Diagnosis: Provides definitive identification of genetic cause
- Family Planning: Enables informed reproductive decisions
- Personalized Management: Guides appropriate medical interventions
- Early Intervention: Facilitates timely treatment planning
- Genetic Counseling: Supports understanding of inheritance patterns
Understanding Your Test Results
Our comprehensive genetic counseling helps interpret your results:
- Positive Result: Confirms HOXA13 gene mutation and diagnosis of Hand-Foot-Genital Syndrome
- Negative Result: Suggests alternative causes for symptoms
- Variant of Uncertain Significance: Requires additional family studies
- Carrier Status: Identifies individuals at risk of passing mutation to offspring
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test | $500 USD | $700 USD |
Test Specifications
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
- Methodology: Next Generation Sequencing (NGS) Technology
- Specialty: Pediatrics and Genetics
- Disease Category: Dysmorphology
Pre-Test Requirements
Before testing, we require:
- Complete clinical history of the patient
- Genetic counseling session to create family pedigree chart
- Documentation of affected family members with similar symptoms
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible genetic testing services for patients nationwide.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your family’s future. Our HOXA13 Gene Guttmacher Syndrome NGS Genetic DNA Test provides the answers you need for informed healthcare decisions. Contact our genetic specialists today to schedule your comprehensive evaluation.
Call or WhatsApp: +1(267) 388-9828 to book your appointment or learn more about our genetic testing services. Our compassionate team is ready to guide you through every step of the testing process.
