Neuro-Molecular Diagnostics and Neuro-Biobank

Providing Free of Charge, Molecular Diagnostics for Neuro-Genetic And Neuromuscular Diseases. - One and only in the State Sector.

Over 500 reports issued to date free of charge costing more than 4 million Rupees through grants and donations. The Neuro-Molecular Diagnostics and Neuro-BioBank recruit’s patients for following disorders, and currently offers genetic testing services for Triplet repeat disorders, Neuromuscular Disorders and Stroke.

 

 

Molecular diagnostic Menu;

 

  1. Triplet Repeat Disorders
  • Huntington’s disease
  • Spinocerebellar ataxia (SCA1, SCA2, SCA3, SCA6, SCA 7, SCA 8 and SCA12)
  • Dentatorubral-pallidolusyian atrophy (DRPLA)
  • Friedreich’s ataxia
  • Fragile X syndrome by PCR
  • Myotonic dystrophy Type

 

  1. Neuromuscular Disorders
  • Duchenne Muscular Dystrophy (DMD) for detection of deletions/duplication in Dystrophin Gene by Multiplex PCR and/or MLPA.
  • Becker Muscular Dystrophy (BMD) for detection of deletions/duplication in Dystrophin Gene by Multiplex PCR/ MLPA.
  • Spinal Muscular Atrophy by deletion analysis of Survival Motor Neuron (SMN1) Gene by PCR and/or MLPA.
  • Limb Girdle Muscular Dystrophy, by MLPA

 

  1. Thrombolytic Panel: Mutations that affect the clotting of Blood.
  • Factor V (Leiden)
  • Factor II Prothrombin
  • MTHFR
  • APOE
  • ACE

 

  1. Parkinson’s Disease