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;
- 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
- 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
- Thrombolytic Panel: Mutations that affect the clotting of Blood.
- Factor V (Leiden)
- Factor II Prothrombin
- MTHFR
- APOE
- ACE
- Parkinson’s Disease