Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome…. 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.
Fibroblast Growth Factor receptor 2 gene
7,245 THB
SKU :
MD-NLB045
Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
Lab Categories : Blood, Bone Deformities, Family History, Genetic Disorders, Lab Test, PCR + DNA Sequencing, Pediatric
Diseases : Genetic Disorders
Symptoms : Bone Deformities
Habits : Family History
Age Groups : Pediatric
Specimens : Blood
Diagnostic Methods : DNA Sequencing, PCR
| Also Known As | FGFR2 Gene Sequencing |
|---|---|
| Specimen | EDTA whole blood 10 ml (minimum 6 ml) |
| Turnaround Time | 30 Days |
| Test Code | MD-NLB045 |
| Test Type | Special |
| Related Tests | Genetic Panel |
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
Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
293,930 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
Gene-agnostic parallel sequencing test to identify genetic mutations associated with cancer.
212,459 THB