Find and Order Laboratory Tests
Invitae Epilepsy Panel:
59,080 THB
Genetic testing for hereditary epilepsy and seizure disorders.
EDTA Blood 6-10 ml + Request form + Clinical history . Kit BML BML SPM Invitae
Neurology Panel
10622
Fatty Acid Profile Essential:
30,816 THB
Analyzes essential fatty acids to assess nutritional status and metabolic health.
Fasting serum 2 mL (Minimun Vol 0.2 mL) 1. Patient should fast overnight (12-14 hours). 2. Patient must not consume any alcohol for 24 hours before the specimen is drawn.
Metabolic Panel
10607
Invitae Long QT Syndrome Panel:
59,080 THB
Detects mutations associated with long QT syndrome, a hereditary heart rhythm disorder.
EDTA Blood 6-10 ml Panel + Request form + Clinical history
Cardiology Panel
10623
Infliximab Quantitation:
36,368 THB
Measures infliximab drug levels to optimize dosing for conditions like Crohn’s disease and rheumatoid arthritis.
serum 1 ml
Drug Monitoring Panel
10608
Invitae Prostate Cancer HRR Panel:
34,736 THB
Detects mutations in genes associated with homologous recombination repair (HRR) in hereditary prostate cancer.
EDTA Blood 6-10 ml Panel + Request form + Clinical history . Kit BML BML SPM Invitae
Oncology Panel
10624
Autosomal recessive polycystic kidney disease:
107,100 THB
Genetic test for ARPKD, a disorder causing kidney and liver problems, especially in children.
EDTA whole blood 6 mL
Genetic Panel
10609
Invitae Frontotemporal Dementia with C9orf72 Panel:
67,176 THB
Genetic testing for frontotemporal dementia, focusing on the C9orf72 gene.
EDTA Blood 6-10 ml + Request form + Clinical history
Neurology Panel
10625
Exome for undiagnosed disease:
105,000 THB
Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
EDTA blood 6 ml (3 ml for children < 8 years)
Genetic Panel
10610
Alpha 1-antitrypsin deficiency:
78,400 THB
Genetic test to detect mutations causing alpha-1 antitrypsin deficiency, which leads to liver and lung disease.
EDTA whole blood 6 mL
Genetic Panel
10611
Hearing loss panel:
107,100 THB
Comprehensive genetic panel for detecting mutations linked to hereditary hearing loss.
EDTA whole blood 6 mL
Genetic Panel
10612
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