Neuro Genetics

Find the genetic cause behind complex neurological conditions.

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What is Neuro Genetics?

Many neurological conditions, from developmental delays to movement disorders, have a genetic basis. Our comprehensive neurology panel uses advanced genetic testing to identify DNA changes linked to inherited neurological disorders, enabling accurate diagnosis and informed decisions on care, management and family planning.

Which neurological conditions can be diagnosed?

  • Developmental delay and intellectual disability
  • Autism spectrum disorders
  • Epilepsy and seizure disorders
  • Neuromuscular disorders (e.g., muscular dystrophy, SMA)
  • Neurodegenerative disorders (e.g., Alzheimer’s, Huntington’s)
  • Movement disorders (e.g., Parkinsonism, dystonia, ataxia)

Who can consider testing ?

  • Children with developmental delay, intellectual disability, or autism spectrum disorders
  • Individuals with unexplained neurological symptoms (e.g., seizures, movement disorders, muscle weakness)
  • Individuals with a family history of neurological conditions
  • Those seeking a confirmed diagnosis for better management and family planning

Tests offered by OneDNA

Comprehensive Neurology Panel

For conditions like: Epilepsy, Seizure disorders, Alzheimer’s, Parkinson’s, Autism, Intellectual disability, etc.

  • Methodology: NGS
  • Sample Type: Blood (EDTA)
  • TAT: 4 weeks

Chromosomal microarray

For conditions like: Autism, Intellectual disability, GDD, microdeletion/duplication syndromes, etc.

  • Methodology: Microarray
  • Sample Type: Blood (EDTA)
  • TAT: 3 weeks

Fragment Analysis (Repeat expansion)

For conditions like: Fragile X, Huntington’s, SCA, FRDA, Myotonic Dystrophy (DMPK, ZFN9), etc.

  • Methodology: TP-PCR
  • Sample Type: Blood (EDTA)
  • TAT: 2–3 weeks

MLPA/ MS-MLPA

For conditions like: DMD, SMA, Prader-Willi/Angelman, etc.

  • Methodology: MLPA
  • Sample Type: Blood (EDTA)
  • TAT: 2–3 weeks

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Why choose OneDNA

Comprehensive Coverage

Comprehensive testing across both molecular and cytogenetic platforms

Accredited Laboratories

NABL & CAP accredited lab

Support & Care

End-to-end support including genetic counselling and report guidance.

Early & Accurate

High accuracy with advanced technologies and stringent quality controls

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Frequently Asked Questions

In many cases, there may be an underlying genetic cause. This test helps uncover it with clarity.

It provides clarity for ongoing care, risk assessment, and future family planning.

If a genetic finding is identified, testing may be recommended for close relatives.

It helps confirm whether a genetic condition is involved and supports more informed clinical decisions.

A simple blood sample is usually all that’s required.

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