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Gnathostoma Ab:
3,750 THB
Detects antibodies against Gnathostoma, a parasitic infection.
Serum 2 ml. or CSF 3-5 mL
Parasitology Panel
10334
Abdominal Pain Gnathostomiasis Antibody Test Parasitic Infections Travel History
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
Oculopharyngeal muscular dystrophy:
7,770 THB
Detects mutations associated with oculopharyngeal muscular dystrophy.
EDTA whole blood 10 ml
Genetic Panel
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)
Neurology Panel
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)
Autoimmune Panel
10324
Autoimmune Disorders None PLA2R Antibody Test Proteinuria Swelling
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