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CDKN1C Gene IMAGE Syndrome NGS Genetic DNA Test

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

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The CDKN1C Gene IMAGE Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that detects mutations in the CDKN1C gene associated with IMAGE syndrome. This advanced Next-Generation Sequencing (NGS) test provides crucial diagnostic information for individuals presenting with characteristic features of this rare genetic disorder. IMAGE syndrome (Intrauterine growth restriction, Metaphyseal dysplasia, Adrenal hypoplasia congenita, and Genital anomalies) is a complex condition affecting multiple body systems. The test is particularly valuable for pediatric patients showing developmental abnormalities, growth restrictions, and endocrine disorders. At only $500 USD, this specialized genetic test offers families and healthcare providers definitive diagnostic clarity, enabling appropriate medical management and informed family planning decisions. Results are typically available within 3-4 weeks from sample collection.

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CDKN1C Gene IMAGE Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for IMAGE Syndrome

The CDKN1C Gene IMAGE Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic tool designed to identify mutations in the CDKN1C gene, which are responsible for IMAGE syndrome. This rare genetic disorder affects multiple body systems and requires precise genetic confirmation for accurate diagnosis and management. Our advanced Next-Generation Sequencing technology provides comprehensive analysis of the CDKN1C gene, delivering reliable results that guide clinical decision-making and family planning.

What Does This Test Measure?

This specialized genetic test specifically targets and analyzes the CDKN1C gene using sophisticated NGS technology to detect:

  • Point mutations and small insertions/deletions in the CDKN1C gene
  • Genetic variants associated with IMAGE syndrome development
  • Inheritance patterns and familial risk assessment
  • Specific mutations affecting cell cycle regulation and growth control

Who Should Consider This Test?

This genetic test is recommended for individuals presenting with symptoms suggestive of IMAGE syndrome, including:

  • Newborns and children with intrauterine growth restriction
  • Patients showing metaphyseal dysplasia or skeletal abnormalities
  • Individuals with adrenal hypoplasia congenita or endocrine disorders
  • Patients exhibiting genital anomalies or developmental abnormalities
  • Family members of individuals diagnosed with IMAGE syndrome
  • Couples with family history of similar genetic conditions planning pregnancy

Key Benefits of CDKN1C Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Definitive Diagnosis: Confirms or rules out IMAGE syndrome with high accuracy
  • Family Planning: Enables informed reproductive decisions and genetic counseling
  • Early Intervention: Facilitates timely medical management and treatment planning
  • Risk Assessment: Identifies carrier status and familial inheritance patterns
  • Peace of Mind: Provides clarity and reduces diagnostic uncertainty

Understanding Your Test Results

Our comprehensive genetic report includes detailed interpretation of your results:

  • Positive Result: Indicates the presence of a CDKN1C gene mutation associated with IMAGE syndrome, requiring specialized medical follow-up
  • Negative Result: Suggests no detectable mutation in the CDKN1C gene, though clinical correlation remains essential
  • Variant of Uncertain Significance: Identifies genetic changes requiring further investigation and family studies
  • Carrier Status: Determines if an individual carries one copy of the mutation without showing symptoms

Test Pricing Information

Test Name Discount Price Regular Price
CDKN1C Gene IMAGE 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: Pediatric Genetics
  • Department: Genetics
  • Disease Category: Dysmorphology

Pre-Test Requirements

Before undergoing testing, we recommend:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create a detailed family pedigree
  • Discussion of testing implications and potential outcomes
  • Informed consent process understanding the benefits and limitations

Nationwide Testing Availability

We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your family’s future. Our CDKN1C Gene IMAGE Syndrome NGS Genetic DNA Test provides the definitive answers you need for informed medical decisions and family planning. With our discounted price of only $500 USD and comprehensive genetic analysis, you can access world-class diagnostic services without financial burden.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to guide you through every step of the testing process and provide the clarity your family deserves.