Molecular Diagnostics & DNA Testing
DNA Labs India | Diagnostic Tests
Molecular Diagnostics & DNA Testing
Clinical Overview
Sub-category mapping under 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.
Tests
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...