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Copper in Blood:

1,404 THB

Measures copper levels in the blood, used to diagnose Wilson’s disease and copper toxicity.
Serum 2 ml
10361
Fatigue Jaundice None Serum Copper Test Wilson’s Disease

Pharmacogenetics for NUDT15:

6,785 THB

Detects NUDT15 gene variants that affect thiopurine drug metabolism, particularly in Asians.
EDTA Whole blood 3-6 ml.
10346
Adverse Drug Reactions Drug Sensitivity Medication Use NUDT15 Genotyping

Pharmacogenetics CYP3A5:

6,000 THB

Detects CYP3A5 gene variants, affecting drug metabolism, including tacrolimus.
EDTA whole blood 5 ml (minimum 3 ml)
10362
Adverse Drug Reactions CYP3A5 Genotyping Drug Sensitivity Medication Use

Pharmacogenetics for Warfarin:

7,350 THB

Detects genetic variations in CYP2C9 and VKORC1 that influence warfarin metabolism and dosing.
EDTA whole blood 5 ml (minimum 3 ml)
10347
Bleeding Bruising CYP2C9 for Warfarin Drug Sensitivity Medication Use Warfarin Sensitivity

Whole Exome Sequencing Trio analysis:

143,500 THB

Analyzes the exome of a patient and both parents (trio analysis) to detect genetic disorders.
EDTA Whole blood Proband >3 ml + Requisition Form and Consent *** Proband ***
10363
Birth Defects Developmental Delays Family History Family Whole Exome Test Genetic Disorders WES Trio Analysis

Adenovirus IgM:

1,485 THB

Detects IgM antibodies to adenovirus, used for diagnosing recent adenovirus infection.
serum 1 ml or Clotted blood 5 ml
10348
Adenovirus Antibody IgM Fever None Respiratory Issues Viral Infections

Ganglioside Antibody IgG:

4,750 THB

Detects IgG antibodies to gangliosides, helping in diagnosing autoimmune neuropathies like Guillain-Barré syndrome.
serum 2-4 ml
10364
Anti-GD1a Antibody Test Autoimmune Disorders Ganglioside IgG Test Muscle Weakness Neurological Disorders None Numbness

Glomerular Basement Membrane Antibody:

2,769 THB

Detects antibodies against the glomerular basement membrane, used to diagnose Goodpasture syndrome.
Serum 2 ml
10349
Blood in Urine GBM Antibody Test Kidney Disease None

Primary Torsion Dystonia genetics study:

3,458 THB

Detects mutations associated with primary torsion dystonia, a movement disorder.
EDTA whole blood 6-10 ml
10365
Family History Genetic Disorders Muscle Cramps Torsion Dystonia Genetic Test Twisting

Ganglioside Antibody IgM:

4,750 THB

Detects IgM antibodies to gangliosides, often used in diagnosing Guillain-Barré syndrome and other neuropathies.
serum 2-4 ml
10350
Anti-GM1 Antibody Test Autoimmune Disorders Ganglioside IgM Test Muscle Weakness Neurological Disorders None Numbness

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