What is Spinal Muscular Atrophy (SMA)?
SMA carrier testing is a genetic test used to determine if a person carries a gene for Spinal Muscular Atrophy (SMA). SMA is a neuromuscular disorder that causes muscle weakness and wasting.
Why Spinal Muscular Atrophy (SMA)is required?
· Family History: If you or your partner have a family history of SMA, carrier testing can help you understand your risk of having a child with the condition.
· Planning a Family: If you are planning to have a family and are concerned about SMA, carrier testing can provide information about your risk and options for genetic counseling and prenatal testing.
which are the method of Spinal Muscular Atrophy (SMA)?
SMA carrier testing typically involves a blood test. The blood sample is analyzed for the presence of specific genetic mutations associated with SMA.
who should go for Spinal Muscular Atrophy (SMA)?
· Individuals with a family history of SMA
· Couples planning to have children
· Individuals who are concerned about their risk of carrying the SMA gene
What are the results of Spinal Muscular Atrophy (SMA)?
The results of an SMA carrier test can be:
- Carrier: You carry one copy of the SMA gene.
- Non-Carrier: You do not carry the SMA gene.
- Unknown: The test was unable to determine your carrier status.
What are the components of Spinal Muscular Atrophy (SMA)?
The components of an SMA carrier test typically include:
- Blood Sample: A blood sample is drawn from your vein.
- Genetic Analysis: The blood sample is analyzed for the presence of specific genetic mutations associated with SMA.
- Results: The results of the test will indicate whether you are a carrier, a non-carrier, or if the test was unable to determine your carrier status.
