Pediatrics Genetic Testing

Personalized Care for Your Child’s Health

Early Detection and Proactive Health Management for Children

Your child’s health is shaped by their unique genetic blueprint, influencing their growth, development, and susceptibility to certain conditions. Pediatrics genetic testing uncovers inherited risks, providing insights into developmental delays, metabolic disorders, and childhood diseases. With personalized genetic insights, you can customize treatments, implement preventive strategies, and optimize care for your child’s unique needs, empowering you to support their health and well-being from an early age.

Why Choose Pediatrics Genetic Testing?

  • Early Detection: Identify genetic risks for childhood conditions before symptoms appear.
  • Personalized Care Plans: Tailored solutions for developmental, metabolic, and genetic disorders.
  • Family Health Insights: Understand hereditary risks and guide family planning decisions.
  • Improved Outcomes: Early intervention and targeted care for better long-term health.

Who Should Consider Pediatrics Genetic Testing?

  • Parents with a family history of genetic disorders or childhood diseases.
  • Children experiencing developmental delays, growth issues, or unexplained symptoms.
  • Families of children diagnosed with metabolic disorders, congenital anomalies, or rare diseases.
  • Parents seeking to understand their child’s genetic risks for proactive health management.
  • Anyone looking to support their child’s health with science-backed insights.

Common Pediatric Conditions We Screen For

Highly Recommended

  • Comprehensive Epilepsy Panel
  • Comprehensive Hearing Loss and Deafness Panel
  • Retinal Dystrophy Panel
  • Primary Immunodeficiency Panel
  • Comprehensive Short Stature Syndrome Panel
  • Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel
  • Bone Marrow Failure Syndrome Panel
  • Macrocephaly / Overgrowth Syndrome Panel
  • Comprehensive Immune and Cytopenia Panel
  • Noonan Syndrome Panel

Cardiology

  • Comprehensive Cardiology Panel
  • Congenital Structural Heart Disease Panel
  • Long QT Syndrome (LQTS) Panel
  • Noonan Syndrome Panel
  • Pulmonary Artery Hypertension (PAH) Panel

Dermatology

  • Ectodermal Dysplasia Panel
  • Epidermolysis Bullosa Panel
  • Ichthyosis Panel
  • Neurofibromatosis Panel
  • Tuberous Sclerosis Panel

Ear, Nose & Throat

  • Branchio-Oto-Renal (BOR) Syndrome Panel
  • Comprehensive Hearing Loss and Deafness Panel
  • Non-Syndromic Hearing Loss Panel
  • Pendred Syndrome Panel
  • Stickler Syndrome Panel
  • Waardenburg Syndrome Panel

Endocrinology

  • Abnormal Genitalia/ Disorders of Sex Development Panel
  • Comprehensive Monogenic Diabetes Panel
  • Hypothyroidism and Resistance to Thyroid Hormone Panel
  • Hypoglycemia, Hyperinsulinism and Ketone Metabolism Panel
  • MODY Panel

Gastroenterology

  • Cholestasis Panel
  • Congenital Diarrhea Panel
  • Gastrointestinal Atresia Panel
  • Hirschsprung Disease Panel
  • Pancreatitis Panel

Hematology

  • Bleeding Disorder/Coagulopathy Panel
  • Bone Marrow Failure Syndrome Panel
  • Comprehensive Immune and Cytopenia Panel
  • Congenital Neutropenia Panel
  • Diamond-Blackfan Anemia Panel
  • Fanconi Anemia Panel
  • Hereditary Leukemia Panel

Hereditary Cancer

  • Hereditary Leukemia Panel
  • Hereditary Pediatric Cancer Panel
  • Neurofibromatosis Panel
  • Tuberous Sclerosis Panel

Immunology

  • Bone Marrow Failure Syndrome Panel
  • Chronic Granulomatous Disease Panel
  • Comprehensive Immune and Cytopenia Panel
  • Primary Immunodeficiency Panel
  • Primary Immunodeficiency (PID) and Primary Ciliary Dyskinesia (PCD) Panel
  • Severe Combined Immunodeficiency Panel

Ophthalmology

  • Albinism Panel
  • Bardet-Biedl Syndrome Panel
  • Cataract Panel
  • Leber Congenital Amaurosis Panel
  • Microphthalmia, Anophthalmia and Anterior Segment Dysgenesis Panel
  • Retinal Dystrophy Panel

Malformations

  • Cleft Lip/Palate and Associated Syndromes Panel
  • Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel
  • Comprehensive Short Stature Syndrome Panel
  • Craniosynostosis Panel
  • Macrocephaly / Overgrowth Syndrome Panel
  • Osteogenesis Imperfecta Panel

Metabolic Disorders

  • Comprehensive Metabolism Panel
  • Fatty Acid Oxidation Syndrome Panel
  • Glycogen Storage Disorder Panel
  • Hyperphenylalaninemia Panel
  • Lysosomal Disorders and Mucopolysaccharidosis Panel
  • Peroxisomal Disorders Panel
  • Mitochondrial Disorders
  • Mitochondrial DNA Depletion Syndrome Panel

Nephrology

  • Bartter Syndrome Panel
  • Ciliopathy Panel
  • Cystic Kidney Disease Panel
  • Hypophosphatemic Rickets Panel
  • Joubert Syndrome Panel
  • Polycystic Kidney Disease Panel
  • Primary Ciliary Dyskinesia Panel
  • Renal Malformation Panel

Neurology

  • Comprehensive Epilepsy Panel
  • Comprehensive Muscular Dystrophy / Myopathy Panel
  • Epileptic Encephalopathy Panel
  • Leukodystrophy and Leukoencephalopathy Panel
  • Neuronal Migration Disorder Panel

Pulmonology

  • Bronchiectasis Panel
  • Central Hypoventilation and Apnea Panel
  • Interstitial Lung Disease Panel
  • Neonatal Respiratory Distress – Surfactant Dysfunction Panel

Comprehensive Genes List

A4GALT, A4GNT, AAAS, AADAC, AADACL2, AAGAB, AANAT, AARS, AARS2, AASS, ABAT, ABCA1, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA5, ABCA7, ABCB1, ABCB11, ABCB4, ABCB5, ABCB6, ABCB7, ABCC1, ABCC11, ABCC12, ABCC2, ABCC3, ABCC4, ABCC6, ABCC8, ABCC9, ABCD1, ABCD3, ABCD4, ABCG1, ABCG2, ABCG5, ABCG8, ABHD1, ABHD12, ABHD5, ABI3BP, ABL1, ABL2, ABO, ABRAXAS1, ACACA, ACACB, ACAD10, ACAD11, ACAD8, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACAN, ACAT1, ACAT2, ACBD5, ACBD6, ACCS, ACE, ACHE, ACKR1, ACKR3, ACLY, ACMSD, ACO2, ACOX1, ACP1, ACP2, ACP5, ACP6,

How It Works?

  1. Consultation: Discuss your child’s symptoms, family history, and concerns with a pediatric genetic specialist.
  2. Sample Collection: Provide a simple saliva or blood sample for DNA analysis.
  3. Advanced Genetic Analysis: State-of-the-art testing detects key genetic mutations linked to childhood health.
  4. Personalized Report: Receive a detailed, easy-to-understand report with actionable insights.
  5. Expert Guidance: Work with pediatricians and genetic counselors to create a tailored care plan.

Why Choose Us?

  • Cutting-Edge Technology: Advanced genetic sequencing for precise and reliable results.
  • Expert Team: Board-certified pediatricians and genetic counselors guiding you every step of the way.
  • Privacy Assurance: Your child’s genetic data is protected with strict confidentiality policies.
  • Compassionate Care: Dedicated to your child’s comfort, well-being, and long-term health.