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Fibroblast Growth Factor receptor 2 gene:

7,245 THB

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Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.

EDTA whole blood 10 ml (minimum 6 ml)

10322

Bone Deformities Family History FGFR2 Gene Sequencing Genetic Disorders

Urine for Organic Acid:

10,878 THB

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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

10291

Developmental Delay Metabolic Disorders None Organic Aciduria Test

Thrombophilia MTHFR:

3,250 THB

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Detects MTHFR mutations, used to assess risk for thrombophilia.

EDTA whole blood 6 ml + clinical history

10292

Blood Clots Family History Genetic Disorders MTHFR Mutation Test

Tricyclic Antidepressants:

2,990 THB

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Monitors levels of tricyclic antidepressants, used to ensure therapeutic drug levels.

serum 1 ml or random urine 10 ml or gastric content 10 ml, EDTA Plasma (Whole blood 3 5 ml) Sodium Heparin plasma and Oxalate plasma

10293

Drug Monitoring None Psychiatric Medications TCA Level Test

Voriconazole level:

3,750 THB

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Measures voriconazole levels, used to monitor antifungal therapy.

Lithium heparine 3-5 ml. or Plasma 1-1.5 ml.

10294

Antifungal Drug Monitoring Antifungal Therapy Drug Monitoring None

von Willebrand Factor:

5,500 THB

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Measures von Willebrand factor antigen, used to diagnose von Willebrand disease.

Citrate plasma 1 ml x 3 tubes

10295

Bleeding Coagulation Disorders Easy Bruising None vWF Antigen Test

Urine free Cortisol:

1,458 THB

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Measures cortisol levels in urine, used to assess adrenal function.

Urine 24 Hrs., No preservative (10 mL)

10296

Endocrine Disorders Fatigue None Urine Cortisol Test Weight Gain

Iodine:

1,512 THB

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Measures iodine levels, used to assess thyroid function and iodine deficiency.

Random urine 5 mL (Protect from light)

10297

Fatigue None Nutritional Deficiency Urine Iodine Test Weight Gain

CADASIL:

11,400 THB

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Detects mutations in the NOTCH3 gene, linked to CADASIL syndrome.

EDTA whole blood 10 ml

10298

CADASIL Genetic Test Family History Genetic Disorders Migraine Stroke

SCA type 1,2,3:

8,505 THB

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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.

EDTA whole blood 10 ml (minimum 6 ml)

10299

Family History Genetic Disorders Spinocerebellar Ataxia Panel Uncoordinated Movements