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Influenza B RNA detection:

5,800 THB

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Detects Influenza B RNA, used to diagnose influenza B infection.

Nasopharyngeal wash or aspirate 1 ml (in sterile container)or Nasal swab in VTM

10316

Cough Fever Flu B PCR Test None Respiratory Infections

Oligoclonal Band:

2,295 THB

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Detects oligoclonal bands, used to diagnose multiple sclerosis and other CNS disorders.

Serum 2 ml & CSF 2 ml

10301

Neurological Disorders None Numbness OCB Electrophoresis Tingling

Methemoglobin:

1,120 THB

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Measures methemoglobin levels, used to diagnose methemoglobinemia.

EDTA whole blood 2 ml

10286

Blood Disorders Chemical Exposure Cyanosis Methemoglobinemia Test Shortness of Breath Smoking

Collagen Binding Activity:

2,025 THB

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Assesses von Willebrand factor function, used in diagnosing von Willebrand disease.

Citrate plasma 1 ml

10302

Bleeding Bruising Coagulation Disorders Collagen Assay None

NIPS:

35,200 THB

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Screening for common chromosomal abnormalities using next-generation sequencing technology.

Maternal blood 10 ml in Streck tube (Special kit )

10287

Maternity Non-invasive Prenatal Screening None Prenatal Screening

Factor VIII Assay:

7,350 THB

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Measures Factor VIII levels, used to diagnose hemophilia and other clotting disorders.

Na Citrate plasma 2 ml

10303

Coagulation Disorders Easy Bruising Factor 8 Activity Test Hemophilia None

NIPS+:

59,200 THB

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Detects chromosomal abnormalities, including microdeletions and aneuploidies, using next-generation sequencing.

Maternal blood 10 ml in Streck tube (Special kit )

10288

Maternity Non-invasive Prenatal Screening Plus None Prenatal Screening

T315I mutation for drug resistance:

8,820 THB

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Detects T315I mutation, which confers resistance to certain leukemia treatments.

EDTA whole blood 3 ml or bone marrow 1 ml in EDTA

10304

Chemotherapy Drug Resistance None T315I Resistance Test

Wilson Disease Mutation:

32,400 THB

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Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.

EDTA whole blood 6-10 ml

10289

Family History Genetic Disorders Liver Dysfunction Neurological Symptoms Wilson's Disease Genetic Test

DNA Mitochondria Mutation For MELAS, MERRF, NARP:

7,245 THB

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Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.

EDTA Whole blood 5 ml

10305

Family History Genetic Disorders Mitochondrial Disease Test Muscle Weakness Seizures