What is Warburg Micro Syndrome?

Warburg Micro is a complicated form of Hereditary Spastic Paraplegia, also called SPG69.

What genes cause it?

Changes of the RAB3GAP1, RAB3GAP2, RAB18, or TBC1D20 genes - RAB3GAP1 being the most prevalent
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Types

WARBM1, WARM2, WARBM3, WARBM4 & Martsolf. What do they mean?
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Research

Stay up to date on the latest Warburg Micro Syndrome SPG69 research.
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Epidemiology

Help fnd the cause of outcomes within the Warburg Micro spectrum. Enroll in a Natural History Study near you!
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Last Updated: April 10th, 2022

Disclaimer: Families should consult a medical professional for genetic diagnosis, management and health concerns. We provide external links to help families and caregivers find additional information- this should not imply our endorsement or responsibility for their content.