Next Generation Sequencing Testing

Hereditary Cardio and Pulmonology Disorders

Hereditary heart and lung conditions often develop silently and may not be detected through routine screening. NGS testing for hereditary cardiology disorders helps identify genetic variants linked to cardiomyopathy, pulmonary hypertension, and other inherited cardiac and pulmonary conditions.

This hereditary cardiac genetic test supports early risk detection and genetic screening for pulmonary hypertension and related disorders. Identifying genes linked to heart and lung conditions allows individuals to protect their heart and lungs early and make informed clinical decisions.
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Immunodeficiency Disorders

Inherited immune disorders can impair the body’s ability to fight infections effectively. NGS genetic testing for immunodeficiency disorders provides comprehensive sequencing analysis through an immune disorder NGS panel.

This sequencing test for immunodeficiency disorders helps identify genetic causes of primary immune disorders. Early detection supports better understanding of the body’s defenses and enables proactive health management for individuals with recurrent or severe infections.
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Neurodegenerative Disorders

Genetic factors play an important role in neurodegenerative disease risk. NGS genetic testing for neurodegenerative disorders identifies genetic variants associated with Alzheimer’s disease, Parkinson’s disease, and ALS.

By understanding how NGS identifies brain disorder risks, individuals can gain early insight into cognitive health. This genetic risk test for neurodegenerative diseases supports long term planning and helps protect cognitive function over time.
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Cancer Genetic Testing

NGS cancer genetic testing evaluates inherited mutations associated with increased cancer risk. This includes hereditary cancer NGS panels such as BRCA and multi gene cancer panels used to assess cancer predisposition.

NGS cancer risk analysis helps distinguish hereditary cancer from sporadic cancer. Early knowledge saves lives by enabling proactive screening, preventive strategies, and informed healthcare decisions related to breast, ovarian, colon, and other cancers.
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Diabetes MODY Testing

Our Diabetes MODY Testing uses advanced genetic profiling to detect mutations in genes associated with Maturity-Onset Diabetes of the Young (MODY)—a hereditary form of diabetes often misdiagnosed as type 1 or type 2.

This test helps identify the specific genetic cause of early-onset diabetes, enabling tailored treatment plans, accurate diagnosis, and improved long-term management. Early genetic insights support personalized care, better therapeutic decisions, and more informed family health planning.
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Hereditary Eye Disorders

Inherited eye conditions can affect vision quality and long term eye health. NGS genetic testing for hereditary eye disorders helps identify genetic variants associated with retinal disorders, inherited vision loss, and other ocular conditions.

Early genetic insight supports proactive eye care planning, targeted monitoring, and informed clinical decision making aimed at preserving vision and reducing the risk of progressive visual impairment.
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Hereditary Thyroid Disorders

Genetic factors can influence thyroid function and increase the risk of inherited thyroid disorders. NGS genetic testing for hereditary thyroid disorders helps identify genetic variations associated with thyroid hormone regulation and autoimmune thyroid conditions.

Understanding genetic risk supports early awareness, appropriate monitoring, and proactive management of thyroid related health concerns before complications develop.
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Hereditary Renal Disorders

Inherited kidney conditions can affect long-term renal function and overall health. NGS genetic testing for hereditary renal disorders identifies genetic variants associated with chronic kidney disease, congenital anomalies, and other inherited renal conditions.

Early detection allows for proactive kidney health monitoring, risk reduction strategies, and informed clinical management to prevent progressive renal damage.
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Hereditary ENT Disorders

Genetic factors can contribute to ear, nose, and throat conditions, including hearing loss, sinus disorders, and other hereditary ENT issues. NGS genetic testing for hereditary ENT disorders identifies relevant gene variants linked to these conditions.

Early genetic insight supports timely interventions, preventive care planning, and personalized monitoring to preserve ENT health and prevent long-term complications.
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Hereditary Metabolic Disorders Testing

Our Hereditary Metabolic Disorders Testing uses advanced Next-Generation Sequencing (NGS) technology to analyze multiple genes associated with inherited metabolic conditions. This genetic test helps identify changes in DNA that may disrupt normal metabolic processes—such as energy production, protein breakdown, and biochemical pathways—and lead to inborn errors of metabolism.
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