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CSF3R gene mutations (Exon 14 and Exon 17):

9,723 THB

Detects mutations in the CSF3R gene, which are linked to various blood disorders, including chronic neutrophilic leukemia.

EDTA Whole Blood >= 3 mL or EDTA Bone Marrow >= 3 mL With CBC result

11060

Anemia CSF3R Mutation Test Hematological Disorders Leukemia None Weakness

Frontotemporal dementia (deletion/duplication analysis on MAPT and GRN genes)(CGC genetics):

52,304 THB

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Tests for deletions or duplications in the MAPT and GRN genes, which are associated with frontotemporal dementia.

EDTA whole blood 3 ml

11052

Behavioral Changes Frontotemporal Dementia FTD Genetic Test Memory Loss Neurological Disorders None

IDH1 and IDH2 Mutations:

12,350 THB

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Detects mutations in the IDH1 and IDH2 genes, commonly found in leukemia and brain tumors.

Formalin-fixed, paraffin-embedded (FFPE) tissue block Dx + H&E slide + Pathology report Pathologist review / EDTA Bone marrow EDTA Blood Leukemia CBC

11053

Brain Tumors Fatigue IDH1/IDH2 Mutation Test Leukemia None Weakness Weight Loss

MTHFR gene mutations (C677T and A1298C):

3,750 THB

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Tests for mutations in the MTHFR gene, which are associated with an increased risk of blood clots and cardiovascular disease.

EDTA whole blood >= 3 mL

11054

Blood Clots Fatigue Homocystinuria MTHFR Mutation Test None Thrombosis

Methanol in Urine (HS-GC-MS):

1,120 THB

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Detects methanol levels in urine, used to diagnose methanol poisoning or exposure.

Random Urine 5-10 mL. (End of shift)

11055

Confusion Dizziness Exposure to Chemicals Methanol Poisoning Methanol Urine Test Nausea Toxic Exposure

NMO IgG (Anti -AQP4):

4,325 THB

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Detects anti-AQP4 antibodies, which are used to diagnose neuromyelitis optica, an autoimmune disorder that affects the central nervous system.

serum 1 ml

11051

Autoimmune Disorders Muscle Weakness Neuromyelitis Optica Neuromyelitis Optica Antibody Test None Vision Loss

Pharmacogenetics for Neurology/Psychiatry by N Health:

23,580 THB

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Tests for genetic variations affecting drug metabolism and efficacy in neurology and psychiatry.

EDTA whole blood >= 3 mL

11046

Anxiety Depression Neuro/Psych Pharmacogenetic Test Neurological Disorders None Psychiatric Disorders Seizures

Haemochromatosis Type 1 (HFE gene):

12,920 THB

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Detects mutations in the HFE gene, associated with hereditary hemochromatosis, leading to excessive iron absorption.

EDTA whole blood 5 ml (Minimun Vol 5 ml.)

11047

Abdominal Pain Fatigue Hemochromatosis Hemochromatosis Genetic Test Iron Overload Disorders Joint Pain None

Rickettsia spot fever group PCR:

4,250 THB

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Detects DNA from the Rickettsia group, used to diagnose spotted fever.

EDTA whole blood 2 ml

11048

Exposure to Ticks Fever Headache Rash Rickettsia PCR Rickettsial Infections Spotted Fever

PGT-M for alpha thalassemia (Family and 1st-4th embryos):

207,571 THB

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Preimplantation genetic testing for alpha thalassemia, using linked polymorphic markers to study familial alleles inheritance.

EDTA whole blood >= 3 mL. – EDTA whole blood >= 3 mL. – ( 1 2nd Generations ) EDTA whole blood >= 3 mL. – Embryos:

11049

Alpha Thalassemia Alpha Thalassemia PGT-M Anemia Family Planning Fatigue Genetic Disorders