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Fragile X syndrome:

11,400 THB

Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.
EDTA whole blood 10 ml (minimum 6 ml)
10337
Developmental Delay Family History Fragile X Genetic Test Genetic Disorders

Nemaline Myopathy (ACTA1):

9,555 THB

Identifies mutations in the ACTA1 gene, associated with nemaline myopathy.
EDTA whole blood 6-10 ml.
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)
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.
10307
ALS Symptoms C9ORF72 Gene Test Family History Genetic Disorders Muscle Weakness

Oculopharyngeal muscular dystrophy:

7,770 THB

Detects mutations associated with oculopharyngeal muscular dystrophy.
EDTA whole blood 10 ml
10323
Difficulty Swallowing Drooping Eyelids Family History Genetic Disorders OPMD Genetic Test

Huntington Expansion:

7,770 THB

Detects expansion mutations in the HTT gene, used to diagnose Huntington’s disease.
EDTA whole blood 10 ml (minimum 6 ml)
10308
Cognitive Decline Family History Genetic Disorders Huntington’s Disease Genetic Test Involuntary Movements

Phospholipase A2 Receptor Ab:

6,210 THB

Detects antibodies to PLA2R, used to diagnose membranous nephropathy.
EDTA Plasma 2 ml or Serum 2 ml (Minimum 1 ml)
10324
Autoimmune Disorders None PLA2R Antibody Test Proteinuria Swelling

Busulfan:

4,500 THB

Monitors busulfan levels, used in chemotherapy for cancer treatment.
Heparin plasma 5 ml.
10309
Busulfan Drug Monitoring Chemotherapy Drug Monitoring None

Volatile organic compounds:

3,750 THB

Detects volatile organic compounds, used to assess exposure to toxic chemicals.
Heparin whole blood 5 ml or urine 10-20 ml
10325
Dizziness Nausea Occupational Exposure Toxicology VOC Screening Test

Testing for Beta gene Thalassemia:

7,015 THB

Detects mutations in the beta-globin gene, used for diagnosing beta thalassemia.
EDTA blood 6 ml. + Hb typing result + CBC result
10310
Anemia Beta Thalassemia Genetic Test Family History Fatigue Genetic Disorders

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