Neurology
DNA Labs India | Diagnostic Tests
Neurology
Clinical Overview
Primary medical category for Neurology
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Subcategories
CSF Analysis
Sub-category mapping under Neurology
4 tests →
General Immunology & Serology
Sub-category mapping under Neurology
13 tests →
Autoimmune Diseases
Sub-category mapping under Neurology
3 tests →
Molecular Diagnostics & DNA Testing
Sub-category mapping under Neurology
26 tests →
General Infectious Diseases
Sub-category mapping under Neurology
1 tests →
Routine & Wellness Checks
Sub-category mapping under Neurology
1 tests →
Rare Disease Diagnostics
Sub-category mapping under Neurology
1 tests →
Histopathology & Cytology
Sub-category mapping under Neurology
1 tests →
Audiology & ENT
Sub-category mapping under Neurology
1 tests →
All Tests
Albumin & IgG CSF Test
To evaluate the CSF IgG/Albumin ratio for diagnosing autoimmune and inflammatory neurological disord...
Albumin CSF Test
To assess albumin protein levels in cerebrospinal fluid for diagnosing neurological disorders, evalu...
Beta 2 Transferrin Fluid Test
To detect cerebrospinal fluid (CSF) leaks by identifying the presence of beta-2 transferrin, a prote...
Oligoclonal Bands IgG CSF Test
The purpose of the Oligoclonal Bands IgG CSF Test is to identify oligoclonal bands in cerebrospinal...
Anti NMDA Receptor / Anti-Glutamate Antibody CSF Test
This test is primarily used to diagnose anti-NMDA receptor encephalitis and anti-glutamate antibody...
Anti-MOG (Myelin Oligodendrocyte Glycoprotein) CSF Test
The purpose of the Anti-MOG CSF Test is to detect and quantify anti-MOG antibodies in cerebrospinal...
Ganglioside GD1b Antibody IgG Test
To diagnose autoimmune neuropathies by detecting Ganglioside GD1b IgG antibodies, aiding in the iden...
Ganglioside GD1a Antibody IgM Test
To detect IgM antibodies against ganglioside GD1a in serum, aiding in the diagnosis of autoimmune ne...
Ganglioside GD1a Antibody IgG Test
The purpose of the Ganglioside GD1a Antibody IgG Test is to detect the presence of IgG antibodies ag...
Ganglioside GD1b Antibody IgM Test
To diagnose neurological disorders such as Guillain-Barre Syndrome, Miller Fisher Syndrome, and Bick...
Immunoglobulin IgG CSF Test
To measure IgG levels in cerebrospinal fluid for diagnosing neurological disorders, including multip...
Immunoglobulin IgG Synthesis Index & Rate Test
This test is used to diagnose and monitor Multiple Sclerosis and other autoimmune diseases by measur...
Immunoglobulin Profile CSF Test
The Immunoglobulin Profile CSF Test is performed to evaluate the immune response within the central...
Multiple Sclerosis Panel 2 Test
To aid in diagnosing Multiple Sclerosis, monitor disease progression, and differentiate MS subtypes...
Myasthenia Gravis Panel Test
The Myasthenia Gravis Panel Test is designed to detect the following antibodies: *Acetylcholine Rece...
PTHrP Parathyroid Hormone Related Protein Test
The primary purpose of the Purkinje Cell Cytoplasmic Antibody Type Tr (DNER) test is to identify the...
VGKC (Voltage Gated Potassium Channel) Antibody CSF Test
To diagnose autoimmune neurological disorders such as limbic encephalitis, Morvan's syndrome, acquir...
Anti NMO (Neuromyelitis Optica) Panel CSF Test
To detect the presence of Anti-Aquaporin-4 (AQP4) and Anti-Myelin Oligodendrocyte Glycoprotein (MOG)...
Anti NMDA Receptor / Anti-Glutamate Antibody Serum Test
The Anti NMDA Receptor / Anti-Glutamate Antibody Serum Test is used for diagnosing autoimmune enceph...
Autoimmune Encephalitis Panel CSF Test
The purpose of the Autoimmune Encephalitis Panel CSF Test is to detect specific antibodies in cerebr...
DRPLA (Dentatorubral-Pallidoluysian Atrophy) Gene Analysis Test
The purpose of the DRPLA Gene Analysis Test is to detect CAG repeat expansions in the ATN1 gene, whi...
MERRF (Myoclonic Epilepsy Associated with Ragged Red Fibres) Mutation Detection Test
To identify pathogenic mutations in mitochondrial DNA associated with MERRF syndrome for diagnostic...
Myotonic Dystrophy Comprehensive Profile Test
To diagnose myotonic dystrophy by detecting mutations in the DMPK and ZFN9 genes, aiding in accurate...
KIF7 Gene Acrocallosal Syndrome NGS Genetic Test
The purpose of the KIF7 Gene Acrocallosal Syndrome NGS Genetic Test is to diagnose Acrocallosal Synd...
APTX Gene Ataxia-Oculomotor Apraxia Type 1 NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the APTX gene to diagnose Ataxia-Ocu...
MYF6 Gene Centronuclear Myopathy Type 3 NGS Genetic Test
The purpose of this test is to detect mutations in the MYF6 gene associated with Centronuclear Myopa...
CST3 Gene Cerebral Amyloid Angiopathy NGS Genetic Test
To identify mutations in the CST3 gene that increase the risk of developing cerebral amyloid angiopa...
SCN2A Gene Convulsions, benign familial infantile, 3 NGS Genetic Test
To identify pathogenic mutations in the SCN2A gene that cause benign familial infantile convulsions,...
PRRT2 Gene Convulsions, familial infantile, with paroxysmal choreoathetosis NGS Genetic Test
To diagnose PRRT2 gene mutations associated with familial infantile convulsions and paroxysmal chore...
SGCE Gene DYT11 NGS Genetic Test
The purpose of the SGCE Gene DYT11 NGS Genetic Test is to identify mutations in the SGCE gene for de...
CASK Gene FG syndrome type 4 NGS Genetic Test
To identify mutations in the CASK gene that cause FG syndrome type 4, aiding in diagnosis, managemen...
FXN Gene Friedreich ataxia NGS Genetic Test
The purpose of this test is to diagnose Friedreich Ataxia by detecting mutations in the FXN gene, co...
CSF1R Gene Leukoencephalopathy, diffuse hereditary, with spheroids NGS Genetic Test
The purpose of the CSF1R Gene Leukoencephalopathy NGS Genetic Test is to confirm diagnosis of HDLS b...
CAPN3 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2A NGS Genetic Test
To identify mutations in the CAPN3 gene for accurate diagnosis of Limb-girdle muscular dystrophy typ...
PUS3 Gene Mental retardation, autosomal recessive type 55 NGS Genetic Test
The purpose of this test is to identify mutations in the PUS3 gene that cause autosomal recessive me...
SYP Gene Mental retardation, X-linked type 96 NGS Genetic Test
To accurately diagnose SYP gene mutations causing X-linked mental retardation type 96 through next-g...
DOK7 Gene Myasthenic syndrome, congenital, type 10 NGS Genetic Test
The purpose of this test is to detect pathogenic mutations in the DOK7 gene, which causes congenital...
DRD2 Gene Myoclonic dystonia, DRD2 related NGS Genetic Test
To confirm the presence of DRD2 gene mutations in individuals suspected of having myoclonic dystonia...
NOL3 Gene Myoclonus, familial cortical NGS Genetic Test
The purpose of the NOL3 Gene Myoclonus NGS Genetic Test is to detect mutations in the NOL3 gene that...
GOSR2 Gene Progressive myoclonus epilepsy type 6 NGS Genetic Test
To diagnose Progressive Myoclonus Epilepsy Type 6 by identifying mutations in the GOSR2 gene using N...
KCTD7 Gene Progressive myoclonus epilepsy type 3 NGS Genetic Test
The purpose of this test is to detect mutations in the KCTD7 gene to diagnose Progressive Myoclonus...
ITPR1 Gene Spinocerebellar ataxia type 15 NGS Genetic Test
To diagnose spinocerebellar ataxia type 15 (SCA15) by detecting mutations in the ITPR1 gene using Ne...
FGF14 Gene Spinocerebellar ataxia type 27, autosomal dominant NGS Genetic Test
The purpose of the FGF14 Gene NGS Genetic Test is to diagnose Spinocerebellar ataxia type 27 by iden...
SLC9A9 Gene Autism Susceptibility, Type 16 NGS Genetic Test
The purpose of this test is to identify SLC9A9 gene variants associated with increased susceptibilit...
SMN1 Gene Spinal muscular atrophy type 2 NGS Genetic Test
The purpose of this test is to diagnose Spinal Muscular Atrophy Type 2 by detecting mutations in the...
ZC4H2 Gene Wieacker-Wolff syndrome NGS Genetic Test
To diagnose Wieacker-Wolff Syndrome by detecting mutations in the ZC4H2 gene and provide information...
Lactate CSF Test
The primary purpose of the Lactate CSF Test is to measure lactate concentration in cerebrospinal flu...
Multiple Sclerosis Panel 1 Test
To diagnose Multiple Sclerosis by detecting antibodies in cerebrospinal fluid and serum, aiding in e...
ERLIN1 Gene SPG62, ERLIN1 related NGS Genetic Test
To detect mutations in the ERLIN1 gene for diagnosis of SPG62, enabling clinical management, genetic...
Biopsy Nerve with Special Stains
The purpose of a nerve biopsy with special stains is to evaluate the structural and pathological cha...
Vestibular Hypofunction Test
The primary purpose of the Vestibular Hypofunction Test is to determine whether a patient has vestib...