ARTHROGRYPOSIS AND CONGENITAL MYASTHENIC SYNDROME
A genetic test to screen for mutations associated with arthrogryposis and congenital myasthenic syndrome. It helps diagnose inherited neuromuscular and musculoskeletal conditions. The panel provides insights into genetic causes of muscle weakness and joint deformities.
Also known asArthrogryposis And Congenital Myasthenic Syndrome Gene Panel Arthrogryposis And Congenital Myasthenic Syndrome Gene Panel
Test details
Preparations
No special preparations needed
Test included
ARTHROGRYPOSIS AND CONGENITAL MYASTHENIC SYNDROME includes 1 parameter
- Arthrogryposis And Congenital Myasthenic Syndrome
Test code
G530
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Amniotic Fluid | Plain Sterile Vaccutainer | 3 ML |
| Peripheral Blood | Others | 3 ML |
Specimen stability information
Amniotic Fluid, Peripheral Blood
Collection instructions
Age, Gender & Clinical History are Mandatory.
Specimen rejection criteria
Test run frequency
Every Day TIME - 08:00
Turn around time
28 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
ARTHROGRYPOSIS AND CONGENITAL MYASTHENIC SYNDROME
Package price
₹22000
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₹22000