MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE
Myotonic dystrophy is an autosomal dominant disorder characterized mainly by muscular dystrophy cataracts, hypogonadism, frontal balding, and ECG changes. Myotonic dystrophy Type 2 (DM2), is rare and generally manifests with milder signs and symptoms than DM1.
Parameter(s) covered : 4
Report Frequency: Sample Mon by 11 am; Report Fri
Special Instruction: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Price : ₹ 8600.00
Parameters
- DMPK Gene CTG Repeats
- Myotonic Dystrophy Type 2
- ZNF9 Gene CCTG Repeats Allele 1
- ZNF9 Gene CCTG Repeats Allele 2