Australian National Spinal Muscular Atrophy Registry
The Australian National Spinal Muscular Atrophy (SMA) Registry provides Australian families with an opportunity to improve the outcomes of individuals affected by spinal muscular atrophy.
The Registry collates a patient’s SMA gene sequence and clinical information about their disease. The Registry is a tool for clinicians and clinical trial sponsors to quickly identify patients suitable for clinical studies, particularly for those therapeutic strategies that target specific genetic defects. Potentially eligible patients will be informed about new trials and studies through the Registry’s clinical network.
Australian SMA Registry Coordinator
|Adding New Patients to Registry|
Details on how to register can be found on the websites below.
|Please see the website for more information|