Find and Order Laboratory Tests
Trisomy 21 by FISH:
8,505 THB
Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.
1. Heparinized whole Blood 5 mL or 2. EDTA whole Blood 5 mL or 3. Heparin/ EDTA Cord blood 2 mL or 4. Amniotic fluid 15 mL
Prenatal Panel
10423
PML/RARA:
8,400 THB
Detects PML/RARA fusion gene associated with acute promyelocytic leukemia (APL).
1. EDTA bone marrow 3-6 ml + bone marrow smear with Wright’s stain(additional) or 2. EDTA whole blood 6 ml
Leukemia Panel
10392
Anti-IFN -Gamma Autoantibody:
5,938 THB
Detects autoantibodies against interferon gamma, used to diagnose chronic infections and immune disorders.
serum 1 ml Not accept lipemic and Hemolysis sample
Autoimmune Panel
10393
PT Mixing test:
2,756 THB
Measures prothrombin time, used to evaluate coagulation factor deficiencies or inhibitors.
Na Citrate plasma 1 ml
Hematology Panel
10394
DNA analysis for 5-Alpha Reductase Deficiency, 5-ARD:
17,908 THB
Detects mutations in the SRD5A2 gene, used to diagnose 5-alpha reductase deficiency.
EDTA whole blood 10 ml + Request form + Clinical history
Endocrine Panel
10395
Sequencing with Dye 5 Rxn:
7,015 THB
Genetic sequencing test used for various conditions requiring sequence analysis.
EDTA whole blood 6-10 ml
Genetic Panel
10396
OF test for hereditary spherocytosis:
840 THB
Detects hereditary spherocytosis, a genetic disorder causing abnormal red blood cells.
Fresh EDTA whole blood 3 ml
Hematology Panel
10397
Pyruvate kinase:
5,500 THB
Measures pyruvate kinase enzyme activity, used to diagnose pyruvate kinase deficiency, a cause of hemolytic anemia.
EDTA whole blood 3 ml
Hemolytic Anemia Panel
10398
DNA Mitochondria Mutation for LHON:
7,455 THB
Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
EDTA Whole blood 5 ml
Genetic Panel
10399
CD59:
5,175 THB
Detects CD59 protein on red blood cells, used to diagnose paroxysmal nocturnal hemoglobinuria (PNH).
Heparinized whole blood 5-6 mL.
Hematology Panel
10400
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