Clinical Exome Sequencing(CES) + Mitochondrial Genome Sequencing

Clinical Exome Sequencing (CES) + Mitochondrial Genome Sequencing

🧬 Unlock Answers Hidden in Your DNA

Clinical Exome Sequencing (CES) combined with Mitochondrial Genome Sequencing is a comprehensive genetic test that analyzes thousands of disease-causing genes along with the entire mitochondrial DNA to identify inherited disorders, rare genetic conditions, and mitochondrial diseases.

✅ Why is this test done?

• Detects rare inherited genetic disorders
• Identifies mitochondrial DNA mutations
• Helps diagnose unexplained neurological disorders
• Evaluates developmental delay and intellectual disability
• Supports diagnosis of metabolic and neuromuscular diseases
• Assists in personalized treatment and genetic counselling

👨⚕️ Who should consider this test?

• Children with unexplained developmental delays
• Individuals with suspected rare genetic disorders
• Patients with muscle weakness or neurological symptoms
• Families with a history of inherited diseases
• Individuals with unexplained metabolic disorders

⭐ Key Benefits

• Comprehensive analysis of thousands of clinically relevant genes
• Complete mitochondrial genome sequencing
• High diagnostic accuracy
• Early diagnosis for better disease management
• Supports family planning and risk assessment

📋 Sample Required

• Peripheral Blood (EDTA)

⏱️ Turnaround Time

• As per laboratory protocol

📞 Book Your Test Today

Advanced BioCare Laboratories
Accurate Diagnosis • Advanced Genetics • Better Healthcare