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Patient Name Birthdate (YYYYMMDD) Sachs Carrier Screening Program Biochemical Testing Requisition METABOLIC DISEASES LABORATORY Atrium Rm 3634 555 University Ave Toronto ON M5G 1×8 Canada Testing:
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The Tay-Sachs carrier screening program is a genetic screening program designed to identify individuals who carry a gene mutation that could potentially result in Tay-Sachs disease.
There is no requirement to file the Tay-Sachs carrier screening program. However, it is recommended for individuals who are planning to have children or are already pregnant to undergo screening to determine their carrier status.
The exact process for filling out the Tay-Sachs carrier screening program may vary depending on the specific program or healthcare provider. Generally, it involves providing a blood or saliva sample for genetic testing. It is advisable to consult with a healthcare professional or genetic counselor for guidance on how to proceed.
The purpose of the Tay-Sachs carrier screening program is to identify individuals who carry a gene mutation for Tay-Sachs disease. This enables informed reproductive choices, such as genetic counseling, prenatal testing, or alternative family planning options to reduce the risk of having a child with the disease.
The specific information required to be reported on the Tay-Sachs carrier screening program may vary depending on the program or healthcare provider. Generally, it may include personal identification details, medical history, and the results of the genetic screening test.
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