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Scientists are close to understanding what causes Warburg Micro,  a Hereditary Spastic Paraplegia called SPG69. By acting now to fund drug screening, you can change children’s lives for the better.

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Rare disorders

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Types of Hereditary Spastic Paraplegias

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To Fund Drug Discovery for SPG69

The Warburg Micro Research Foundation announces

the Natural history study

This study is tracking the natural course of the disease over time. It’s also looking for important biomarkers that tell us about severity.

If your loved one has been diagnosed with Warburg Micro SPG69, please contact Boston Children’s.
To learn more click here.

Warburg Micro is a complicated form of hereditary spastic paraplegia.

Symptoms include: cataracts, low vision, developmental delay, missed milestones like walking and talking, progressing spasticity, and feeding issues.
warburg micro syndrome

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Check out our list of clinicians and therapy centers and connect with others fighting this disorder.