Pediatrics & Neonatology
DNA Labs India | Diagnostic Tests
Pediatrics & Neonatology
Clinical Overview
Primary medical category for Pediatrics & Neonatology
| 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
Routine & Wellness Checks
Sub-category mapping under Pediatrics & Neonatology
4 tests →
Molecular Diagnostics & DNA Testing
Sub-category mapping under Pediatrics & Neonatology
9 tests →
General Neurology
Sub-category mapping under Pediatrics & Neonatology
1 tests →
All Tests
Newborn Screening Panel 4 Test
The purpose of the Newborn Screening Panel 4 Test is to detect four specific conditions in newborns:...
Newborn Screening Panel Comprehensive Test
The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots c...
Newborn Screening Panel Extended Test
The purpose of the Newborn Screening Panel Extended Test is to screen for a range of disorders inclu...
Newborn Screening Panel 8 Test
The purpose of the Newborn Screening Panel 8 Test is to identify newborns who may have certain metab...
ZIC1 Gene Craniosynostosis type 6 NGS Genetic Test
The purpose of the ZIC1 Gene Craniosynostosis Type 6 NGS Genetic Test is to accurately diagnose Cran...
FGFR2 Gene Crouzon syndrome NGS Genetic Test
To diagnose Crouzon syndrome by detecting pathogenic mutations in the FGFR2 gene using NGS technolog...
CENPE Gene Microcephaly, autosomal recessive type 13 NGS Genetic Test
The purpose of this test is to identify mutations in the CENPE gene that cause autosomal recessive m...
ASPM Gene Microcephaly, autosomal recessive type 5 NGS Genetic Test
To identify mutations in the ASPM gene for definitive diagnosis of autosomal recessive microcephaly...
AGPS Gene Rhizomelic chondrodysplasia punctata type 3 NGS Genetic Test
The purpose of the AGPS Gene Rhizomelic chondrodysplasia punctata type 3 NGS Genetic Test is to diag...
WASHC5 Gene Ritscher-Schinzel syndrome type 1 NGS Genetic Test
To identify mutations in the WASHC5 gene that cause Ritscher-Schinzel Syndrome Type 1, aiding in dia...
chr. 11p15 Gene Silver-Russell syndrome NGS Genetic Test
The purpose of this test is to identify genetic mutations in the chr. 11p15 gene that cause Silver-R...
TWIST1 Gene Craniosynostosis type 1 NGS Genetic Test
To identify mutations in the TWIST1 gene for diagnosis of craniosynostosis type 1, aiding in early i...
FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic Test
To identify mutations in the FLVCR2 gene that cause hydranencephaly, Fowler type, aiding in diagnosi...
TUBB2B Gene Microcephaly, TUBB2B related NGS Genetic Test
To diagnose TUBB2B gene microcephaly by detecting mutations in the TUBB2B gene using NGS technology,...