Find and Order Laboratory Tests

Autosomal recessive polycystic kidney disease:

107,100 THB

Genetic test for ARPKD, a disorder causing kidney and liver problems, especially in children.
EDTA whole blood 6 mL
10609
ARPKD Gene Test Family History Genetic Disorders Kidney Cysts Kidney Disease Panel Liver Fibrosis

Invitae Frontotemporal Dementia with C9orf72 Panel:

67,176 THB

Genetic testing for frontotemporal dementia, focusing on the C9orf72 gene.
EDTA Blood 6-10 ml + Request form + Clinical history
10625
Behavioral Changes Family History FTD with C9orf72 Gene Panel Genetic Testing for FTD Memory Loss Neurodegenerative Disorders

Exome for undiagnosed disease:

105,000 THB

Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
EDTA blood 6 ml (3 ml for children < 8 years)
10610
Family History Genetic Disorders Varies by condition WES Whole Exome Sequencing

Alpha 1-antitrypsin deficiency:

78,400 THB

Genetic test to detect mutations causing alpha-1 antitrypsin deficiency, which leads to liver and lung disease.
EDTA whole blood 6 mL
10611
AATD Gene Test Alpha-1 Deficiency Sequencing Family History Genetic Disorders Liver Disease Respiratory Issues

Hearing loss panel:

107,100 THB

Comprehensive genetic panel for detecting mutations linked to hereditary hearing loss.
EDTA whole blood 6 mL
10612
Deafness Gene Panel Family History Genetic Disorders Genetic Hearing Loss Test Hearing Loss

G6PD deficiency common Asian mutation:

8,400 THB

Screens for common G6PD mutations prevalent in Asian populations, associated with G6PD deficiency.
EDTA whole blood 3-5 ml (2 tubes)
10613
Family History Fatigue G6PD Asian Mutation Panel G6PD Genetic Test Genetic Disorders Hemolytic Anemia

AZF deletion by PCR:

21,420 THB

Detects deletions in the AZF region of the Y chromosome, often related to male infertility.
EDTA whole blood 3 ml
10614
AZF Gene Deletion Test Genetic Disorders Genetic History Infertility Y Chromosome Microdeletion Test

Newborn screening test panel:

32,292 THB

Screens newborns for various metabolic and genetic disorders like galactosemia, cystic fibrosis, and adrenal hyperplasia.
Dried blood spot collected on Guthrie filter card within 24-72 hours of life
10615
Genetic Disorders Guthrie Test Neonatal Screening Newborns Varies by condition

West Nile Virus PCR:

4,325 THB

Detects West Nile Virus genetic material using PCR in cases of suspected WNV infection.
CSF or serum or EDTA plasma 1 ml
10616
Fever Neurological Symptoms Travel History Viral Infections West Nile Virus Test WNV PCR

VZV DNA Quantitative:

5,819 THB

Quantifies VZV DNA to assess viral load in infections like chickenpox and shingles.
CSF 1 ml or urine 1 ml or EDTA whole blood 3 ml or EDTA plasma
10617
Chickenpox/Shingles PCR Immunocompromised Neurological Symptoms Rash Varicella-Zoster Virus DNA Test Viral Infections

Description:

Alias:

Specimen:

Related Tests:

Filter By Categories

All Categories filter

Diseases Category

Symptoms Category

Lifestyle Category

Age Groups Category

Category by Diagnostic Methods

Category by Specimen

Sorry, no results match your search criteria.

Shopping Cart
Scroll to Top