Neurodevelopment Panels are genetic tests that can provide crucial insights into the underlying causes of conditions like delayed development, neurodegeneration, and movement disorders. By analyzing an individual’s DNA, these tests can identify specific genetic variations associated with these conditions, leading to more accurate diagnoses, personalized treatment plans, and informed medical management decisions.
Test ID | Disorder | Genes |
---|---|---|
NDDT_001 | Brain malformations (eg: Agenesis of the corpus callosum, Dandy-Walker syndrome, Holoprosencephaly, Hydrocephalus, Lissencephaly, Meckel syndrome, Polymicrogyria, Pontocerebellar hypoplasia) | 139 genes |
NDDT_002 | Epilepsy (eg: Epileptic encephalopathy, Infantile spasm (West syndrome), Lennox-Gastaut syndrome, Neuronal ceroid lipofuscinosis) | 97 genes |
NDDT_003 | Macrocephaly | 83 genes |
NDDT_004 | Microcephaly (eg: Aicardi-Goutières syndrome, Coffin-Siris syndrome, Cornelia de Lange syndrome, Seckel syndrome) | 161 genes |
Methodology: | NGS |
Sample Type | Container | Shipping Conditions | Max Transit Time |
---|---|---|---|
Blood | EDTA Tube | 4–8 °C | 72 hrs |
Saliva | Saliva Collection Kit | 4–8 °C | 48 hrs |
Genomic DNA | 1.5 ml Eppendorf Tube | 4–8 °C | 48 hrs |
Dry Blood Spot | Whatmann Paper | RT | 72 hrs |
Cheek/Buccal Swab | Saliva Collection Kit | 4–8 °C | 48 hrs |
21 Days