Chromosomal Microarray CMA 750K High Resolution Test
Comprehensive Genetic Analysis for Precise Diagnosis
The Chromosomal Microarray CMA 750K High Resolution Test represents the gold standard in modern genetic diagnostics, offering unparalleled resolution for detecting chromosomal abnormalities. This advanced molecular cytogenetic technique provides clinicians with detailed insights into genetic variations that traditional methods cannot detect, making it an essential tool for accurate diagnosis and personalized medical management.
What Does the CMA 750K Test Measure?
Our high-resolution chromosomal microarray test detects a wide range of genetic abnormalities with exceptional precision:
- Microdeletions and microduplications as small as 50-100 kilobases
- Copy number variations (CNVs) across all chromosomes
- Chromosomal imbalances and structural rearrangements
- Regions of homozygosity indicating potential recessive disorders
- Submicroscopic chromosomal abnormalities invisible to conventional karyotyping
Who Should Consider This Test?
Clinical Indications and Symptoms
The CMA 750K High Resolution Test is recommended for individuals presenting with:
- Unexplained developmental delays or intellectual disabilities
- Autism spectrum disorders or related neurodevelopmental conditions
- Multiple congenital anomalies affecting multiple organ systems
- Growth abnormalities including failure to thrive or overgrowth
- Dysmorphic features without clear syndromic diagnosis
- History of multiple miscarriages or stillbirths
- Family history of chromosomal abnormalities or genetic disorders
Key Benefits of Chromosomal Microarray Testing
Superior Diagnostic Capabilities
- Higher Resolution: Detects abnormalities 100 times smaller than traditional karyotyping
- Comprehensive Coverage: Analyzes all chromosomal regions simultaneously
- Objective Results: Automated analysis reduces human interpretation errors
- Clinical Utility: Provides actionable information for treatment and management
- Family Planning: Offers recurrence risk information for future pregnancies
Understanding Your Test Results
Interpretation and Clinical Significance
Your CMA 750K test results will be carefully interpreted by our board-certified genetic specialists:
- Pathogenic Findings: Clearly identified genetic abnormalities with known clinical significance
- Variants of Uncertain Significance (VUS): Genetic changes requiring further clinical correlation
- Benign Variations: Common polymorphisms with no clinical impact
- Normal Results: No detectable chromosomal abnormalities within test resolution
Our genetic counselors provide comprehensive result explanations and guidance on next steps, ensuring you fully understand the implications for medical management and family planning.
Test Details and Pricing
| Test Information | Details |
|---|---|
| Test Name | Chromosomal Microarray CMA 750K High Resolution Test |
| Discount Price | $450 USD |
| Regular Price | $700 USD |
| Turnaround Time | 15 days |
| Sample Type | Blood |
| Testing Method | Affymetrix CytoScan 750K Microarray |
Nationwide Accessibility
We have branches conveniently located across the United States, serving patients in all 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 regardless of location.
Take the Next Step Toward Genetic Clarity
Don’t let unanswered genetic questions affect your health decisions. Our Chromosomal Microarray CMA 750K High Resolution Test provides the comprehensive answers you need for informed medical management. Contact us today to schedule your test and take advantage of our special discounted pricing.
Call or WhatsApp us at +1(267) 388-9828 to book your appointment or speak with our genetic specialists.
Important Pre-Test Requirement: A duly filled Genomic Microarray Requisition Form (Form 19) is mandatory for all test orders. Please ensure your healthcare provider completes this form before your appointment.

