Help Us

Find a treatment

Scientists are close to understanding what causes Warburg Micro,  a Hereditary Spastic Paraplegia called SPG69. Give our children a chance, fund drug discovery.

Latest Press release

UCD Researchers awarded grant to study WMS

0 +

Rare disorders


Types of Hereditary Spastic Paraplegias

$ 0 K

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

Newly Diagnosed?

You are not alone.

Find resources for your family.
Check out our list of clinicians and therapy centers and connect with others fighting this disorder.