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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
Genetic Panel
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
Neurology Panel
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)
Genetic Panel
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
Genetic Panel
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
Genetic Panel
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)
Hematology Panel
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
Genetic Panel
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
Metabolic and Genetic Panel
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
Viral Panel
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
Viral Panel
10617
Chickenpox/Shingles PCR Immunocompromised Neurological Symptoms Rash Varicella-Zoster Virus DNA Test Viral Infections
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