Find and Order Laboratory Tests
Dysferlinopathy (Dysferlin):
38,400 THB
Detects mutations in the dysferlin gene associated with muscular dystrophy (dysferlinopathy).
EDTA whole blood 10 ml (minimum 6 ml)
Muscular Dystrophy Panel
10951
BKV Viral Load by Real-time PCR:
5,865 THB
Measures the viral load of BK virus in blood, plasma, or urine using real-time PCR for transplant patients or those with kidney issues.
2 ml of EDTA whole blood / 500 ul of EDTA Plasma/ Urine 1-3 ml
Viral Load Testing
10936
HIV-1 Proviral Drug Resistant for ultralow viral load (PI):
10,290 THB
Detects drug resistance mutations in the protease region of HIV-1 for patients with low viral loads.
EDTA whole blood 3-5 mL (With HIV-1 RNA viral load between less than 20 – 1,000 copies/ml)
HIV Drug Resistance Testing
10937
Mitragynine (KRATOM) in Urine by Rapid test:
1,050 THB
Detects the presence of mitragynine (Kratom) in urine for substance use screening using a rapid test.
Urine
Drug Screening
10938
Prenatal diag for Alpha Thal( Father ):
6,325 THB
Detects common alpha thalassemia mutations using GAP-PCR and ARMS PCR in prenatal testing (paternal).
EDTA Whole blood 5 ml
Prenatal Screening
10939
Multiplex Specific IgE Profile (ALEX) 295 allergens:
29,700 THB
Measures specific IgE levels for 295 different allergens using the ALEX allergy platform.
serum 1 ml (Minimum volume 500 uL)
Allergy Testing
10940
Anti Acetylcholine Receptor (Anti AChR) and muscle specific tyrosine kinase (Anti MuSK):
5,750 THB
Detects antibodies against acetylcholine receptors and MuSK, associated with myasthenia gravis.
Serum 2 ml
Neuromuscular Disorder Panel
10941
Gliadin IgA and tissue transglutaminase IgA by Immunochromatography:
2,120 THB
Detects IgA antibodies against gliadin and tissue transglutaminase to evaluate celiac disease.
– Serum 1 mL or – EDTA/Heparinized/Sodium citrate whole blood 1 mL
Celiac Disease Panel
10926
Xmn I Polymorphism for thalassemia:
7,176 THB
Detects the XmnI polymorphism in the HBG2 gene, which can influence the severity of beta-thalassemia.
EDTA whole blood >= 3 mL with Hemoglobin typing result
Hemoglobinopathy Testing
10942
Deafness (Cx 26) Mutation:
7,770 THB
Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness.
EDTA whole blood 6-10 ml (minimum 5 ml)
Genetic Hearing Loss Panel
10927
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