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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
Bartonella Antibody Panel, IgG and IgM:
23,508 THB
Detects IgG and IgM antibodies against Bartonella species, used to diagnose infections like cat scratch disease.
Serum 1 ml,Frozen
Infectious Disease Panel
10597
Animal Exposure Bartonella Henselae Antibody Test Cat Scratch Disease Test Fever Infectious Diseases Lymphadenopathy
OncoHeme Next-Generation Sequencing for Myeloid Neoplasms:
154,980 THB
Comprehensive genetic test to identify mutations in myeloid neoplasms like leukemia and myelofibrosis.
Extracted DNA: 100 mcL at 20 ng/mcL concentra- tion (From EDTA blood or EDTA bone marrow)
Genetic Cancer Panel
10598
Anemia Cancer Fatigue Myeloid Cancer NGS Panel None OncoHeme NGS
Myelin Oligodendrocyte Glycoprotein:
38,448 THB
Detects antibodies to myelin oligodendrocyte glycoprotein, used in diagnosing demyelinating disorders like MOGAD.
Serum 2 ml
Neurological Autoimmune Panel
10599
Autoimmune Disorders MOG Antibody Test MOGAD Test None Visual Disturbances Weakness
Copeptin proAVP, Plasma:
30,375 THB
Measures levels of copeptin, a marker for arginine vasopressin secretion, used in diagnosing water-balance disorders.
EDTA plasma 0.5 ml, Minimum Volume 0.3 ml. Patient Preparation: For water-deprived testing, have the patient fast and thirst for at least 8 hours (no liquids, including water, are allowed)
Hormonal Panel
10600
AVP Plasma Test Copeptin Test Electrolyte Imbalance Endocrine Disorders Thirst Water Deprivation
Vasoactive Intestinal Polypeptide:
32,480 THB
Measures VIP levels, often elevated in cases of VIPoma, a rare neuroendocrine tumor.
EDTA plasma 2 mL
Endocrine Panel
10601
Diarrhea Endocrine Disorders Flushing Hormonal Disorders Vasoactive Peptide Test VIP Test
Alpha thalassemia 2:
5,500 THB
Detects alpha-thalassemia using amniotic fluid and parental blood samples, often during pregnancy.
Amniotic fluid 16-20 ml with maternal blood in EDTA tube 3 ml (Penetrate at the gestational age of 18-20 weeks and must be attached the father and mother’s result of DNA typing every time.)
Genetic Carrier Panel
10586
Alpha-Thal 2 PND Anemia Family History Fatigue Genetic Disorders Prenatal Alpha Thalassemia Test
Insulin Antibodies:
26,100 THB
Measures insulin antibodies, used to assess autoimmune reactions in diabetes.
Serum 2 ml
Diabetes Panel
10602
Autoimmune Disorders Diabetes Family History Hyperglycemia IAA Insulin Autoantibody Test
PND for Beta thalassemia:
6,440 THB
Detects beta-thalassemia in fetuses using amniotic fluid and parental blood samples.
Amniotic fluid 8-10 ml with father and mother blood in EDTA tube 3 ml (Penetrate at the gestational age of 18-20 weeks and must be attached the father and mother’s result of DNA typing every time.)
Genetic Carrier Panel
10587
Anemia Beta-Thal PND Family History Fatigue Genetic Disorders Prenatal Beta Thalassemia Test
Vitamin D Level:
21,924 THB
Measures the concentration of vitamin D in the blood to evaluate bone health and overall vitamin D status.
Serum 2 ml (protected from light)
Nutritional Panel
10603
25-Hydroxyvitamin D Bone Pain Diet Fatigue Metabolic Disorders Sunlight Exposure Vitamin D Test
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