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Methemoglobin:
1,120 THB
Measures methemoglobin levels, used to diagnose methemoglobinemia.
EDTA whole blood 2 ml
Hematology Panel
10286
Blood Disorders Chemical Exposure Cyanosis Methemoglobinemia Test Shortness of Breath Smoking
Collagen Binding Activity:
2,025 THB
Assesses von Willebrand factor function, used in diagnosing von Willebrand disease.
Citrate plasma 1 ml
Coagulation Panel
10302
Bleeding Bruising Coagulation Disorders Collagen Assay None
NIPS:
35,200 THB
Screening for common chromosomal abnormalities using next-generation sequencing technology.
Maternal blood 10 ml in Streck tube (Special kit )
Prenatal Panel
10287
Maternity Non-invasive Prenatal Screening None Prenatal Screening
Factor VIII Assay:
7,350 THB
Measures Factor VIII levels, used to diagnose hemophilia and other clotting disorders.
Na Citrate plasma 2 ml
Coagulation Panel
10303
Coagulation Disorders Easy Bruising Factor 8 Activity Test Hemophilia None
NIPS+:
59,200 THB
Detects chromosomal abnormalities, including microdeletions and aneuploidies, using next-generation sequencing.
Maternal blood 10 ml in Streck tube (Special kit )
Prenatal Panel
10288
Maternity Non-invasive Prenatal Screening Plus None Prenatal Screening
T315I mutation for drug resistance:
8,820 THB
Detects T315I mutation, which confers resistance to certain leukemia treatments.
EDTA whole blood 3 ml or bone marrow 1 ml in EDTA
Hematology Panel
10304
Chemotherapy Drug Resistance None T315I Resistance Test
Wilson Disease Mutation:
32,400 THB
Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.
EDTA whole blood 6-10 ml
Liver Panel
10289
Family History Genetic Disorders Liver Dysfunction Neurological Symptoms Wilson's Disease Genetic Test
DNA Mitochondria Mutation For MELAS, MERRF, NARP:
7,245 THB
Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
EDTA Whole blood 5 ml
Neurology Panel
10305
Family History Genetic Disorders Mitochondrial Disease Test Muscle Weakness Seizures
DNA Mitochondria Mutation for KSS/CPEO:
11,025 THB
Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
EDTA Whole blood 5 ml
Neurology Panel
10290
Family History Genetic Disorders Kearns-Sayre Syndrome DNA Test Muscle Weakness Vision Problems
Urine for Organic Acid:
10,878 THB
Measures organic acids in urine, used to diagnose inborn errors of metabolism.
First morning urine 30 ml (frozen if cannot perform in same day) minimum 10 ml
Metabolic Panel
10291
Developmental Delay Metabolic Disorders None Organic Aciduria Test
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