Neurology Genetic Testing

Personalized Insights for Brain and Nerve Health

Early Detection and Targeted Care for Neurological Disorders

Your brain and nervous system health are fundamentally tied to your DNA, influencing everything from cognitive function and movement to sensory processing and emotional well-being. Neurology genetic testing reveals inherited risks, offering insights into conditions like epilepsy, neurodegenerative diseases, and neuromuscular disorders. With personalized genetic insights, you can tailor treatments, adopt preventive measures, and optimize care for your unique profile, empowering you to protect and enhance your neurological health.

Why Choose Neurology Genetic Testing?

  • Early Detection: Identify genetic risks for neurological disorders before symptoms progress.
  • Personalized Treatment Plans: Tailored solutions for epilepsy, movement disorders, and cognitive decline.
  • Family Health Insights: Understand hereditary risks and help family members take preventive steps.
  • Improved Quality of Life: Manage neurological health effectively and enjoy a healthier, more fulfilling life.

Who Should Consider Neurology Testing?

  • Individuals with a family history of neurological disorders, seizures, or movement disorders.
  • People experiencing unexplained muscle weakness, numbness, or coordination problems.
  • Those diagnosed with epilepsy, neuropathy, or neurodevelopmental conditions.
  • Patients with early-onset dementia, Parkinson’s disease, or ALS.
  • Children and adults with intellectual disabilities, autism spectrum disorders, or neurodegenerative.

Common Neurological Conditions We Address

  • Amyotrophic Lateral Sclerosis Panel
  • Ataxia Panel
  • Ataxia panel with FMR1 repeat expansion New
  • Autism Spectrum Disorders Panel
  • Beyond Paediatric Epilepsy Panel – for Europe
  • Cerebral Cavernous Malformation Panel
  • Charcot-Marie-Tooth Neuropathy Panel
  • Coenzyme q10 Deficiency Panel
  • Collagen Type VI-Related Disorders Panel
  • Comprehensive Epilepsy Panel
  • Comprehensive Muscular Dystrophy / Myopathy Panel
  • Congenital Myasthenic Syndromes Panel
  • Creatine Metabolism Deficiency Panel
  • Dementia Panel
  • Dystonia Panel
  • Emery-Dreifuss Muscular Dystrophy Panel
  • Epileptic Encephalopathy Panel
  • Holoprosencephaly Panel
  • Idiopathic Generalized and Focal Epilepsy Panel
  • Leukodystrophy and Leukoencephalopathy Panel
  • LGMD and Congenital Muscular Dystrophy Panel
  • Lissencephaly Panel
  • Macrocephaly / Overgrowth Syndrome Panel
  • Metabolic Epilepsy Panel
  • Metabolic Myopathy and Rhabdomyolysis Panel
  • Microcephaly and Pontocerebellar Hypoplasia Panel
  • Migraine Panel
  • NCL and Progressive Myoclonic Epilepsy Panel
  • Nemaline Myopathy Panel
  • Neuro-Ophthalmology Panel
  • Neuronal Migration Disorder Panel
  • Parkinson Disease Panel
  • Periodic Paralysis Panel
  • Polymicrogyria Panel
  • Porphyria Panel
  • Septo-Optic Dysplasia Panel
  • Spastic Paraplegia Panel
  • Spinal Muscular Atrophy Panel
  • Tuberous Sclerosis Panel
  • X-linked Intellectual Disability Panel
  • X-linked Intellectual Disability Panel with

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 symptoms, family history, and concerns with a neurology 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 neurological health.
  4. Personalized Report: Receive a detailed, easy-to-understand report with actionable insights.
  5. Expert Guidance: Work with neurologists 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 neurologists and genetic counselors guiding you every step of the way.
  • Privacy Assurance: Your genetic data is protected with strict confidentiality policies.
  • Compassionate Care: Dedicated to your comfort, well-being, and long-term health.