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Diagnosing SMA early is critical

Knowing the signs of spinal muscular atrophy (SMA) can speed up time to diagnosis, which can ultimately improve outcomes.

The diagnosis of neuromuscular disorders, including SMA, in young children is often delayed, preventing patients from receiving the management and services they require.2

With treatment now available for SMA, its relative effectiveness may depend on being able to identify patients early enough to initiate treatment before irreversible neuronal loss occurs.1,3

The Red Flags Checklist offers healthcare professionals a simple reminder to help recognise the early signs of SMA and other neuromuscular disorders (NMDs).

Download SMA red flags checklist
Download NMDs red flags checklist

If you suspect SMA or another NMD in any of your patients, refer immediately to your local neuromuscular clinic

A simple genetic test can confirm the diagnosis of SMA so treatment can be initiated earlier to improve outcomes.1

Find your nearest neuromuscular clinic using our Clinic Finder.

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Learn more and gain CPD points with an accredited module on paediatric neuromuscular disorders

  • 1-hour online education module
  • RACGP accredited for two category 2 QI&CPD points
  • Developed in collaboration with a panel of Australian paediatric neuromuscular experts
Access here
References
  1. D’Amico D et al. Orphanet J Rare Dis 2011; 6: 71.
  2. Lurio J et al. Am Fam Physician 2015; 91: 38–4.
  3. Finkel RS et al. N Engl J Med 2017; 377: 1723–32.