Advanced Research in Genetic & Metabolic Disorders
NIRMAN – Navi Mumbai Institute of Research specializes in the diagnosis and treatment of genetic and metabolic disorders in pediatric patients, offering world-class expertise and care.
Diagnostic Tests Done
Accuracy Results
What We Offer
Advanced Diagnostic Solutions for Genetic & Metabolic Disorders
Providing accurate, research-backed testing to support early detection and better clinical outcomes.
Genetic & Molecular Testing
About NIRMAN
Pioneering Research in Metabolic & Genetic Disorders
NIRMAN – Navi Mumbai Institute of Research was established on December 15th, 1998 by Dr. Anil B. Jalan and his colleagues with a specific focus on the study and treatment of genetic and metabolic aspects of neurological disorders in the pediatric age group.
We have expanded our scope to encompass various genetic disorders including Bad Obstetric History, Genodermatosis, and Liver Disorders. Our institute collaborates with prestigious European centers of excellence, bringing world-class expertise to our patients.
- Established in 1998 with a vision for specialized genetic research
- Collaboration with leading European centers of excellence
- Comprehensive approach to genetic and metabolic disorders
- State-of-the-art diagnostic capabilities
- Specialized care for pediatric patients
- International recognition and publications
Patients Served
Years of Excellence
Our Expertise
World-Class Specialization in Metabolic Medicine
Trained at leading European centers, we bring cutting-edge expertise in diagnosing and treating rare genetic and metabolic disorders.
Neurometabolic Disorders
Specialized diagnosis and treatment of various neurometabolic conditions affecting the nervous system.
Newborn Screening
Early detection programs for metabolic disorders in critically ill newborns.
Molecular Diagnostics
Advanced molecular diagnosis of genetic disorders using cutting-edge technology.
Mitochondriopathies
Expert analysis and management of mitochondrial energy metabolism disorders.
Lysosomal Storage Disorders
Comprehensive testing and treatment for enzyme deficiency disorders.
Peroxisomal Disorders
Comprehensive diagnostic and treatment facilities
Trained at prestigious European institutions including:
University of Vienna (Austria) • University of Graz (Austria) • Neurometabolic Centre of Nijmegen (Holland) • BIRD Institute (Italy) • AMC Amsterdam
Diagnostic Services
Comprehensive Testing & Analysis
We offer a wide range of specialized diagnostic tests for genetic and metabolic disorders, utilizing state-of-the-art laboratory facilities and methodologies.
Metabolic Studies
- Ammonia
- Lactate
- Blood Sugar Levels
- Sr. Uric Acid
- Sr. Cholesterol
Newborn Screening
- Thyroid Screening T4 / TSH
- 17 OHP
- G 6 PD
- GALT enzyme
- Total Galactose
Special Enzymes
- Alfa Fucosidase
- Alfa Galactosidase
- Alfa Glucosidase
- Alfa Mannosidase
- Aryl Sulphatase A
Special Metabolites
- Chitotriosidase
- CCL 18
- Gl – 3 : Lyso Gl – 3
- PPT / NCL – 1
- TPP / NCL – 2
Special Tests
- Transferrin Isoelectric Focusing for CDG
- ADA / PNP Enzymes
-
HGPRT / APRT Enzymes
-
Sr. Homocysteine
Immunological Tests
- Anti – Gliadin Ab – Ig G
- Anti – Gliadin Ab – Ig A
- Anti– Endomyseal Ab –IgA
- Anti– Parietal cell Ab – IgA
Profiles
- Galactosemia Screening
- TLC Sugar, GALT & Galactose
- Methionine / MTHFR Mutation Analysis
Biochemical Tests
- 1st Focused Course on “congenital Disorders of Glycosylation” Training in Basic & Advanced Laboratory
Why Choose NIRMAN
Excellence in Metabolic Care
Combining international expertise, advanced diagnostics, and compassionate care to deliver exceptional outcomes for our patients.
Connect With NIRMAN’s Genetic Specialists
Connect with NIRMAN’s genetic specialists for expert evaluation, guidance, and care in metabolic and genetic disorders.