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
SKU :
MD-NLMM123
Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
365,781 THB
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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 |
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