Pediatrics Genetic Testing

Pediatrics Genetic Testing is a specialized diagnostic tool used to identify genetic disorders and inherited conditions in children. It analyzes a child’s DNA to detect mutations, chromosomal abnormalities, or genetic variations that may cause developmental delays, congenital anomalies, metabolic disorders, or other health issues. Early detection through genetic testing can guide personalized treatment plans, improve disease management, and provide valuable information for family planning. This testing helps pediatricians understand the root cause of unexplained symptoms, supports early intervention, and enhances long-term health outcomes for affected children. It is increasingly essential in modern pediatric healthcare.

Why Choose This Pediatrics Genetic Testing?

Choosing Pediatrics Genetic Testing offers invaluable benefits by providing precise insights into a child’s genetic makeup, enabling early and accurate diagnosis of hereditary or developmental conditions. This testing helps tailor treatments and interventions specific to the child’s needs, improving health outcomes and quality of life. It also assists families in understanding potential risks, guiding informed decisions about care and future pregnancies. By identifying underlying genetic causes, pediatricians can avoid unnecessary tests and treatments, speeding up the path to effective management. Overall, it empowers healthcare providers and families with crucial knowledge to support the child’s health and development comprehensively.

When Is It Used?

To diagnose unexplained developmental delays or intellectual disabilities in children.
When a child shows symptoms of a suspected inherited metabolic or genetic disorder.
To investigate congenital anomalies or birth defects present at or after birth.
When there is a family history of genetic conditions or hereditary diseases.
To identify the cause of recurrent unexplained illnesses or neurological problems.
For newborn screening to detect treatable genetic disorders early.

Who Should Consider Pediatrics Genetic Testing?

Pediatrics Genetic Testing is recommended for children who exhibit unexplained medical symptoms, developmental delays, or congenital anomalies that suggest a genetic cause. Families with a history of genetic disorders or inherited conditions should also consider testing to better understand potential risks. Additionally, pediatricians may suggest testing for children with recurrent health issues or neurological symptoms that are difficult to diagnose. Early genetic insights can help tailor treatments and guide family planning decisions, making it a valuable tool for both affected children and their families.

You should consider this test if:

Children with unexplained developmental delays or intellectual disabilities
Children born with congenital anomalies or birth defects
Children with symptoms of metabolic or genetic disorders
Families with a known history of genetic conditions
Children with dChildren with recurrent, unexplained illnesses or neurological symptomsevelopmental delays or regression. Adults with unexplained fatigue, hearing loss, or vision changes.
Newborns for early screening of treatable genetic disorders

How We Work

How is the Test Performed?

Our Services

Just a few of the many health issues we screen for

Down Syndrome

A chromosomal disorder causing developmental delays, intellectual disability, and distinct physical features due to an extra chromosome 21.

Rett Syndrome

A neurodevelopmental disorder affecting mostly girls, causing loss of motor skills, speech, and coordination after early normal development.

Fragile X Syndrome

An inherited condition causing intellectual disability, behavioral challenges, and autism-like symptoms, linked to a mutation on the X chromosome.

Duchenne Muscular Dystrophy

A genetic disorder causing progressive muscle weakness, typically appearing in early childhood, due to mutations in the dystrophin gene.

Smith-Lemli-Opitz Syndrome

A developmental disorder caused by cholesterol metabolism issues, leading to intellectual disability and physical abnormalities.

Beckwith-Wiedemann Syndrome

A growth disorder present at birth, causing large body size, organ enlargement, and increased risk of childhood tumors like Wilms tumor.

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