Tests can be carried out to check if you or your child has spinal muscular atrophy (SMA), or if you're at risk of having a child with the condition.
Speak to a GP if you're planning a pregnancy and:
- you've had a child with SMA before
- you have a history of the condition in your family
- your partner has a history of the condition in their family
The GP may refer you for genetic counselling to help you understand the risk of your child having SMA. You can have a genetic test to see if you have the faulty gene linked to the condition.
If you're at risk of having a child with SMA, talk to your genetic counsellor about your options.
These may include:
- getting pregnant and waiting to see if your child is born with SMA, or having tests during pregnancy to see if they will have it
- using donated sperm or eggs to get pregnant
- pre-implantation genetic diagnosis (PGD) – where a woman's eggs are fertilised in a laboratory and the resulting embryos are tested for SMA before being put in the womb
If you're pregnant and there's a risk you could have a child with SMA, tests can be carried out to check for the condition.
The 2 main tests are:
- chorionic villus sampling (CVS) – a sample of cells from the placenta are tested, usually during weeks 11 to 14 of pregnancy
- amniocentesis – a sample of amniotic fluid is tested, usually during weeks 15 to 20 of pregnancy
Both these tests can slightly increase your chances of a miscarriage.
If tests show your baby is likely to have SMA, talk to your doctor about what this means and what your options are.
If you or your child has typical symptoms of SMA, a genetic blood test can be done to confirm the condition.
You may also be asked if anyone in your family has a condition that affect their nerves and muscles.
A physical examination may be done to look for signs of SMA or similar conditions.
Very occasionally, other tests may be needed, too. For example:
- electromyography – thin needles are inserted into a muscle to detect how well it's working
- muscle biopsy – a small sample of muscle is taken for analysis
The charity Spinal Muscular Atrophy UK provides more information and advice if your child has recently been diagnosed with SMA.