NX GEN SEQ, OPHTHALMOPLEGIA
Ophthalmoplegia is a progressive condition characterized by weakness of the eye muscles. It typically appears in adults between 18 to 40 years of age and slowly worsens over time. Mutations in several different genes on different chromosomes are associated with Ophthalmoplegia. This test is useful for the genetic determination of this disorder.
Parameter(s) covered : 1
Report Frequency: Sample Daily by 9 am; Report 45 Working days
Special Instruction: Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Price : ₹ 24500.00
Parameters
- Nx Gen Seq Ophthalmoplegia