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Laboratory: Genomics
Test Name:
MYOTONIC DYSTROPHY TYPE 1 (DM1) - DMPK GENE - (B)
Test Code: MD
Clinical Information:
For asymptomatic patients, a prior consult with the WRHA Genetics & Metabolism Program is required.
Prenatal diagnosis requires prior consultation with Molecular Diagnostic Lab.
For more information see: 
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=myotonic-d
Collection Devices:
Specimen Required:
Blood: 8.0 mL
Pediatric Blood: 3.0 mL

Specimen must be kept at room temperature. Pediatric volume for infants only.
Referral:

Testing may be performed on amniotic fluid (4.0 mL required) or cultured amniocytes.
Requisition:
Reference Values:
An interpretive report will be sent.
Availability:
Within 8 Weeks
See Also:
More Information:
Do NOT centrifuge.  Specimen is forwarded to Health Sciences Centre - MS5 for analysis.  Store and ship specimens at room temperature.  Specimens sent for Molecular tests are not to be used for other tests (ie. CBC).