Single Gene Testing

Single Gene Testing is a genetic test that examines a specific gene to identify mutations or changes that may cause a particular inherited condition or disease. This test focuses on one gene at a time, making it highly targeted and precise. It is typically used when there is a known family history or symptoms strongly suggest a disorder linked to a single gene, such as cystic fibrosis or Huntington’s disease. By detecting gene mutations, single gene testing helps in diagnosis, risk assessment, and guiding treatment or management options for affected individuals and their families.

Why Choose This single gene Testing?

Single Gene Testing offers precise and targeted analysis by focusing on a specific gene associated with your symptoms or family history, ensuring highly accurate results. It enables early diagnosis of genetic conditions, often before symptoms appear, allowing for timely and effective intervention. This testing supports personalized care by guiding treatment plans tailored to your unique genetic makeup. Additionally, it provides valuable information for family planning by identifying inherited risks, helping individuals make informed decisions. Compared to broader genetic panels, single gene testing is often more cost-effective and delivers clearer, easier-to-interpret results, reducing uncertainty for patients and healthcare providers alike.

When Is It Used?

When there is a strong family history of a specific genetic disorder
To confirm a diagnosis based on clinical symptoms
For individuals showing signs of a single gene condition
To assess risk for inherited diseases before symptoms appear
For prenatal or carrier screening in family planning
To guide personalized treatment or management decisions

Who Should Consider Single Gene Testing?

Single Gene Testing is ideal for individuals with a strong personal or family history of a specific genetic condition known to be caused by a single gene mutation. It is especially useful when symptoms clearly point to a particular disorder, or when a known mutation has already been identified in a family member. This focused approach ensures high accuracy, quicker results, and can guide treatment or preventive care effectively.

You should consider this test if:

Individuals with symptoms linked to a known single-gene disorder
Those with a family member already diagnosed with a specific gene mutation
Parents seeking carrier testing for a specific inherited condition
Patients requiring confirmation of a clinical diagnosis
Individuals planning for children with a known genetic risk in the family
Individuals undergoing targeted treatment where specific gene mutations affect drug response
People seeking predictive testing for late-onset genetic conditions like Huntington’s disease

How We Work

How is the Test Performed?

Our Services

Just a few of the many health issues we screen for

Huntington’s Disease

A progressive brain disorder caused by a single gene mutation, leading to uncontrolled movements, cognitive decline, and emotional disturbances in adulthood.

Sickle Cell Anemia

A blood disorder caused by an HBB gene mutation, leading to misshapen red blood cells, pain, organ damage, fatigue, and increased infection risk.

Wilson Disease

An inherited condition where copper accumulates in the body due to mutations in the ATP7B gene, leading to liver and neurological damage.

Thalassemia

An inherited blood disorder causing the body to produce less hemoglobin than normal, leading to anemia, fatigue, and potential organ damage in severe forms.

Canavan Disease

A rare inherited condition caused by ASPA gene mutation that leads to progressive brain damage, severe developmental delays, and shortened life expectancy in affected children.

Gaucher Disease

A genetic disorder caused by GBA gene mutations, leading to fat accumulation in organs, enlarged liver and spleen, bone pain, and blood abnormalities.

Who we Are

Why Choose Us?

State-of-the-Art Digital Lab Experience

Our fully integrated E-Lab platform offers online test ordering, real-time tracking, and secure digital reporting bringing convenience and control to both physicians and patients across the country.

Advanced Diagnostic Technology

From routine blood tests to complex genetic panels, we leverage cutting-edge platforms like NGS, PCR, and AI-powered analytics for maximum accuracy and clinical relevance.

Fast Turnaround, Local Support

With lab facilities based in Florida, we ensure faster processing times and direct access to our expert team. You get timely results backed by responsive, local customer support.

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Comprehensive Thyroid Panel
Comprehensive Thyroid Panel
Food Sensitivity & Allergy Testing (IgG/IgE Panels)
STI/STD Comprehensive Panel (PCR or Blood Tests)
Diabetes Panel (HbA1c, Fasting Glucose, Insulin, C-Peptide)
Autoimmune Disease Panel

Comprehensive Thyroid Panel
Comprehensive Thyroid Panel
Food Sensitivity & Allergy Testing (IgG/IgE Panels)
STI/STD Comprehensive Panel (PCR or Blood Tests)
Diabetes Panel (HbA1c, Fasting Glucose, Insulin, C-Peptide)
Autoimmune Disease Panel

TESTS

NGS TESTING

PCR TESTING

Infectious Disease