Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
PGT-M for common disease
365,781 THB
SKU :
MD-NLMM123
Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
Diseases : Genetic Disorders, Monogenic Diseases
Symptoms : Family History of Genetic Disorders
Habits : Genetic Counseling, IVF
Age Groups : Adults
Specimens : EDTA Whole Blood, Embryo Biopsy
Diagnostic Methods : Linkage Analysis, PCR
| Also Known As | Preimplantation Genetic Testing for Monogenic Diseases |
|---|---|
| Specimen | EDTA whole blood >= 3 mL. – EDTA whole blood >= 3 mL. – ( 1 2nd Generations ) EDTA whole blood >= 3 mL. – Embryos: |
| Turnaround Time | 2 months |
| Test Code | MD-NLMM123 |
| Test Type | Special |
| Related Tests | Preimplantation Genetic Testing,Genetic Counseling |
Related Product
Detects antibodies to desmoglein 1, used to diagnose pemphigus foliaceus, an autoimmune skin disease causing skin blistering.
2,860 THB
Measures specific IgE antibodies to gluten, used to diagnose gluten sensitivity or wheat allergies.
2,600 THB
Measures pregnenolone hormone levels, used to assess adrenal function and hormonal balance.
32,220 THB
Detects chromosomal abnormalities, large deletions or duplications, and uniparental disomy in miscarriage tissue to determine causes of pregnancy loss.
51,200 THB
Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
293,930 THB
Screens for common drugs of abuse using liquid chromatography/tandem mass spectrometry (LC-MS/MS), with detection limits varying by substance.
10,238 THB