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Myotonic dystrophy type 1, DMPK gene:
12,180 THB
Detects mutations in the DMPK gene, used to diagnose myotonic dystrophy type 1.
EDTA blood 6-10 ml
Neurology Panel
10315
DM1 Genetic Test Family History Fatigue Genetic Disorders Muscle Weakness
Influenza B RNA detection:
5,800 THB
Detects Influenza B RNA, used to diagnose influenza B infection.
Nasopharyngeal wash or aspirate 1 ml (in sterile container)or Nasal swab in VTM
Respiratory Panel
10316
Cough Fever Flu B PCR Test None Respiratory Infections
Entamoeba histolytica Ab:
3,250 THB
Detects antibodies to Entamoeba histolytica, used to diagnose amebiasis.
Serum (Only) 2 ml
Parasitology Panel
10317
Abdominal Pain Amebiasis Antibody Test Diarrhea Parasitic Infections Travel History
Bacteria : molecular identification:
6,720 THB
Identifies bacterial species using 16S rDNA sequencing, useful for difficult-to-culture bacteria.
fluid or pus from sterile site in sterile container or purified colonies or EDTA whole blood 3 ml
Infectious Diseases Panel
10318
16S rDNA PCR for Bacteria Abscess Fever Infectious Diseases None
Filaria IgG4 Ab:
2,430 THB
Detects IgG4 antibodies to filarial parasites, used to diagnose filariasis.
Serum 2 ml.
Parasitology Panel
10319
Filaria Antibody Test Parasitic Infections Skin Rashes Swelling Travel History
Metachromatic Leukodystrophy, MLD:
11,875 THB
Detects mutations associated with metachromatic leukodystrophy, a disorder affecting the nervous system.
EDTA whole blood 5 – 10 ml.
Neurology Panel
10320
Family History Genetic Disorders MLD Genetic Test Muscle Weakness Vision Problems
Protein C gene mutation:
13,300 THB
Detects mutations in the protein C gene, used to diagnose protein C deficiency and related clotting disorders.
EDTA whole blood 6-10 ml
Hematology Panel
10321
Blood Clots Coagulation Disorders Family History Protein C Deficiency Test
Nemaline Myopathy (ACTA1):
9,555 THB
Identifies mutations in the ACTA1 gene, associated with nemaline myopathy.
EDTA whole blood 6-10 ml.
Neurology Panel
10306
ACTA1 Genetic Test Family History Genetic Disorders Hypotonia Muscle Weakness
Fibroblast Growth Factor receptor 2 gene:
7,245 THB
Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
EDTA whole blood 10 ml (minimum 6 ml)
Genetic Panel
10322
Bone Deformities Family History FGFR2 Gene Sequencing Genetic Disorders
C9Orf72 expansion:
7,015 THB
Detects expansions in the C9ORF72 gene, linked to ALS and frontotemporal dementia.
EDTA whole blood 6 ml. or EDTA Bone marrow 3 ml.
Neurology Panel
10307
ALS Symptoms C9ORF72 Gene Test Family History Genetic Disorders Muscle Weakness
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