CMA750K – Chromosomal Microarray Analysis

Product Description

CMA750K (Chromosomal Microarray Analysis) is an advanced genetic test designed to detect chromosomal abnormalities, including microdeletions, microduplications, and copy number variations (CNVs) across the genome. This high-resolution test helps in identifying genetic causes associated with developmental delay, intellectual disability, autism spectrum disorders, congenital anomalies, and reproductive disorders.

Using advanced microarray technology, the CMA750K test provides detailed genomic insights with enhanced accuracy and reliability.

Test Highlights

• High-resolution genome-wide analysis
• Detects copy number variations (CNVs)
• Identifies microdeletions and microduplications
• Useful for pediatric, prenatal, and reproductive genetics
• Supports early diagnosis and clinical decision-making

Recommended For

• Developmental delay
• Autism spectrum disorders
• Congenital abnormalities
• Intellectual disability
• Recurrent pregnancy loss
• Infertility evaluation

Sample Required

• Peripheral Blood / Prenatal Sample

Reporting Time

• 10–15 Working Days

Technology Used

• Chromosomal Microarray Platform (750K Resolution)

Why Choose This Test?

• Comprehensive genomic screening
• High diagnostic yield
• Accurate and reliable reporting
• Expert interpretation by specialists

Package Includes

• Sample processing
• Genome-wide analysis
• Detailed clinical report

Note

This test should be interpreted by a qualified healthcare professional along with clinical findings.

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