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Diagnostic Genetic Testing

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Diagnostic Genetic Testing

Diagnostic Genetic Testing

Diagnostic Genetic Testing is a precise and powerful tool used to identify genetic mutations that may be causing or contributing to various medical conditions. This testing helps in diagnosing genetic disorders, providing critical insights for treatment and management, and supporting better health outcomes.

Benefits:

  • Precise Diagnosis: Helps pinpoint the exact genetic cause of a condition, leading to a more accurate diagnosis and avoiding misdiagnoses.
  • Informed Treatment Decisions: Enables healthcare providers to design treatment plans that are specifically suited to the patient’s genetic profile, improving outcomes.
  • Family Health Insights: Provides valuable information for family members who may be at risk, facilitating early detection and preventive care.
  • Genetic Counseling Support: Offers access to genetic counseling to help patients understand their results and implications for their health and family planning.
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Features:

  • Comprehensive Genetic Analysis: Examines specific genes, chromosomes, or DNA sequences to identify mutations or abnormalities linked to genetic disorders.
  • Accurate Diagnosis: Provides a definitive diagnosis for conditions with a suspected genetic cause, such as cystic fibrosis, muscular dystrophy, or hereditary cancers.
  • Personalized Treatment Plans: Offers detailed genetic insights that guide tailored treatment and management strategies.
  • Wide Range of Conditions: Can be used to diagnose a broad spectrum of conditions, from rare genetic disorders to more common hereditary diseases.

Who Should Consider Diagnostic Genetic Testing:

  • Unexplained Symptoms: Individuals with unexplained medical symptoms that may have a genetic basis.
  • Family History: Those with a family history of genetic disorders or hereditary conditions who need a precise diagnosis.
  • Prenatal Concerns: Parents or prospective parents with concerns about passing on genetic conditions to their children.

Frequently Asked Questions (FAQs)

What is Diagnostic Genetic Testing?
Diagnostic genetic testing identifies specific genetic mutations or abnormalities that may be causing a medical condition, helping to diagnose genetic disorders accurately.
What if a genetic mutation is found?
If a genetic mutation is identified, your healthcare provider will explain its implications, discuss treatment options, and provide referrals for genetic counseling if necessary.
Are there any risks associated with the testing?
The testing is generally non-invasive, with minimal physical risks. However, emotional support is available to help you cope with any challenging information the test may reveal.