Molecular Diagnostics | Manovikas Kendra

Centre for Molecular Diagnostics

Unveiling Precision to Empower Health

At Manovikas Kendra, we recognise that assessment encompasses both clinical and molecular aspects. Aids in the diagnostic confirmation of genetic/chromosomal disorders. The Centre also helps in the identification of molecular markers involved with higher disease severity. Our pharmacogenomic based analysis helps in prescribing targeted medication. This reduces treatment induced side effects, often being the cause for treatment discontinuation.

To ensure precise validation of clinical assessments, the Centre for Molecular Diagnostics performs a series of tests recommended by the psychiatrist. These are conducted by a specialized team experienced in working with children with special needs, including phlebotomist, laboratory technicians and research scientists, with final verification by a pathologist

This centre aids in

Blood tests as recommended by the doctor
Chromosomal and other genomic (PCR and RT-PCR based) tests for diagnosing conditions such as Fragile X syndrome, Prader-Willi syndrome, Angelman syndrome, Down syndrome, and others.
Vitamin Deficiency tests.
Pharmacogenomic and nutrigenomic tests based on assessment results.
Neurotransmitter analysis for emotional instability.

Inflammatory marker testing for all the aforementioned conditions.
Diagnostic confirmation of genetic as well as chromosomal disorders.
Identification of molecular markers involved with higher disease severity.
Pharmacogenomic analysis to help in prescribing tailored therapeutic intervention. This reduces the treatment induced side effects, often being a cause for treatment discontinuation.

What We Do

Assessment & Therapy

Brain Function Therapy

Education

Molecular Diagnostics