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Find and Order Laboratory Tests
Mitragynine:
9,177 THB
Detects mitragynine, a compound found in kratom, used for drug screening.
Clotted blood 3-5 mL. or NaF 3-5 mL.
Toxicology Panel
10418
Drowsiness Drug Use Kratom Drug Test Nausea Substance Abuse
FIP1L1-PDGFRA Fusion gene:
7,056 THB
Detects FIP1L1-PDGFRA fusion gene associated with myeloid neoplasms, particularly eosinophilic leukemia.
EDTA whole blood 6 ml or EDTA bone marrow 2 ml
Leukemia Panel
10387
Blood Cancer Easy Bruising Fatigue None PDGFRA Gene Fusion Test
Toluene:
1,288 THB
Measures toluene levels in urine, used to assess occupational or environmental exposure.
Urine 10 ml
Toxicology Panel
10403
Dizziness Fatigue Occupational Exposure Toluene Exposure Test Toxicology
Genetic for Familial Mediterranean Fever:
12,075 THB
Detects mutations in the MEFV gene associated with Familial Mediterranean Fever (FMF), an inflammatory disorder.
EDTA whole blood 10 ml + request form
Genetic Panel
10388
Familial Mediterranean Fever Genetic Test Family History Fever Genetic Disorders Inflammatory Disorders Stomach Pain
Thiocyanate:
2,322 THB
Measures thiocyanate levels, used to assess cyanide exposure from smoking or occupational hazards.
Random Urine end of shift 20 ml
Toxicology Panel
10404
Cyanide Exposure Test Headache Nausea Occupational Exposure Toxicology
Hemophilia B Mutation:
13,300 THB
Detects mutations in the F9 gene, used to diagnose hemophilia B.
EDTA whole blood 10 ml (minimum 6ml)
Hematology Panel
10389
Bleeding Coagulation Disorders Easy Bruising Family History Hemophilia B Genetic Test
Zika IgM:
4,125 THB
Detects IgM antibodies to Zika virus, used to diagnose Zika virus infection.
serum 1 ml
Viral Panel
10405
Fever Rash Travel History Viral Infections Zika Virus IgM Test
Marfan Syndrome:
22,500 THB
Detects mutations in the FBN1 gene, used to diagnose Marfan syndrome.
EDTA whole blood 10 ml
Genetic Panel
10390
Family History Genetic Disorders Heart Problems Marfan Syndrome Genetic Test Tall Stature
PKD1 mutation:
44,800 THB
Detects mutations in PKD1 gene, used to diagnose autosomal dominant polycystic kidney disease (ADPKD).
EDTA whole blood 6-10 ml
Kidney Panel
10391
Abdominal Pain Family History Genetic Disorders Kidney Cysts Polycystic Kidney Disease Genetic Test
PML/RARA:
8,400 THB
Detects PML/RARA fusion gene associated with acute promyelocytic leukemia (APL).
1. EDTA bone marrow 3-6 ml + bone marrow smear with Wright’s stain(additional) or 2. EDTA whole blood 6 ml
Leukemia Panel
10392
APL Fusion Gene PCR Blood Cancer Fatigue Infections None
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